Lpa receptor antagonists and uses thereof

ABSTRACT

The present disclosure relates generally to compounds that bind to Lysophosphatidic Acid Receptor 1 (LPAR1) and act as antagonists of LPAR1. The disclosure further relates to the use of the compounds for the preparation of a medicament for the treatment of diseases and/or conditions through binding of LPAR1, including fibrosis and liver diseases such as non-alcoholic steatohepatitis (NASH), interstitial lung disease (ILD), or chronic kidney disease (CKD).

CROSS-REFERENCES TO RELATED APPLICATIONS

This application claims the benefit under 35 U.S.C. § 119(e) of U.S.provisional application No. 63/034,220, filed on Jun. 3, 2020, and ofU.S. provisional application No. 63/130,242, filed on Dec. 23, 2020,which are hereby incorporated herein by reference in their entiretiesfor all purposes.

FIELD

The present disclosure relates to compounds that bind to and act asantagonists of a lysophosphatidic acid (LPA) receptor, such as LPAR1.The disclosure further relates to the use of the compounds for thetreatment and/or prophylaxis of diseases and/or conditions associatedwith one or more LPA receptors, e.g., an LPAR1 associated disease orcondition.

BACKGROUND

Lysophosphatidic acids (mono-acyl-glycerol-3-phosphate, LPA) are a classof biologically active phospholipids that can be produced fromlysophosphatidyl choline (LPC), e.g., by the enzyme autotaxin. A typicalLPA has a glycerol, an ester-linked fatty acid at the sn-1 position, anda phosphate head group at the sn-3 position. LPA with various fattyacids have been identified, including palmitoyl LPA (16:0), stearoyl LPA(18:0), oleoyl LPA (18:1), linoleoyl LPA (18:2) and arachidonyl LPA(20:4). LPA exerts a wide range of cellular responses, such asproliferation, differentiation, survival, migration, adhesion, invasion,and morphogenesis through a family of rhodopsin-like G protein-coupledreceptors (GPCRs). Six LPA receptors have been been characterized andwere found to differ in their tissue distribution and downstreamsignaling pathways. These six LPA receptors are often referred tointerchangeably as LPAR1-6 (gene) or LPA1-6 (protein). LPA receptormediated signaling has been shown to influence many biological processessuch as wound healing, immunity, carcinogenesis, angiogenesis andneurogenesis.

In vivo studies involving LPA receptor-deficient mice or certain toolcompounds have suggested a potential of LPA receptors as possible drugtargets in a variety of diseases including cancer, fibrosis,inflammation, pain, and cardiovascular diseases. More recently, LPAR1antagonists have been studied clinically in connection with fibroticdisease states such as idiopathic pulmonary fibrosis (IPF) and systemicsclerosis.

A need remains for LPA antagonists with desirable selectivity, potency,metabolic stability, or reduced detrimental effects.

SUMMARY

The present disclosure provides compounds useful as inhibitors ofLysophosphatidic Acid Receptor 1 (LPAR1). The disclosure further relatesto the use of the compounds for the treatment and/or prophylaxis ofdiseases and/or conditions through binding of LPAR1 by said compounds.

In one embodiment, provided herein is a compound of Formula (I),

or a pharmaceutically acceptable salt thereof,

-   wherein:-   R¹ is hydrogen, C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₃₋₁₀    cycloalkyl, 3 to 10 membered heterocyclyl having 1 to 4 heteroatoms    independently selected from nitrogen, oxygen, and sulfur, 6 to 10    membered aryl, or 5 to 10 membered heteroaryl having 1 to 4    heteroatoms independently selected from nitrogen, oxygen, and    sulfur, wherein each alkyl, alkenyl, alkynyl, cycloalkyl,    heterocyclyl, aryl, or heteroaryl is optionally substituted with 1    to 4 R^(1A), which can be the same or different, wherein each R^(1A)    is independently selected from halogen, cyano, nitro, oxo, C₁₋₄    alkyl, C₃₋₁₀ cycloalkyl, 3 to 10 membered heterocyclyl having 1 to 4    heteroatoms independently selected from nitrogen, oxygen, and    sulfur, 6 to 10 membered aryl, 5 to 10 membered heteroaryl having 1    to 4 heteroatoms independently selected from nitrogen, oxygen, or    sulfur, —N(R^(1B1))(R^(1B2)), —O—R^(1B1), —S—R^(1B1),    —C(O)N(R^(1B1))(R^(1B2)), —NR^(1B1)C(O)R^(1B2),    —NR^(1B1)C(O)N(R^(1B2))(R^(1B3)), —S(O)₀₋₂R^(1B1),    —S(O)₂N(R^(1B1))(R^(1B2)), and —NR^(1B1)S(O)₂R^(1B2), wherein each    R^(1B1), R^(1B2) and R^(1B3) is independently hydrogen, C₁₋₆ alkyl    or C₃₋₆ cycloalkyl,    -   wherein each R^(1A) alkyl, cycloalkyl, heterocyclyl, aryl, and        heteroaryl is optionally substituted with 1 to 4 R^(1C), which        can be the same or different, and wherein each R^(1C) is        independently C₁₋₄ alkyl, halogen, cyano, —O—R^(1D1), or        —N(R^(1D1))(R^(1D2)), wherein each R^(1D1) and R^(1D2) is        independently hydrogen or C₁₋₆ alkyl, and    -   wherein each R^(1B1), R^(1B2), and R^(1B3) alkyl and each        R^(1B1), R^(1B2), and R^(1B3) cycloalkyl is optionally        substituted with 1 to 3 halogens; or-   R¹ is —O—R^(1D1) or —N(R^(1D1))(R^(1D2)), wherein each R^(1D1) and    R^(1D2) is independently hydrogen, C₁₋₆ alkyl, or C₃₋₆ cycloalkyl,    wherein each C₁₋₆ alkyl, or C₃₋₆ cycloalkyl is optionally    substituted with 1 to 4 R^(1E), which can be the same or different,    wherein each R^(1E) is independently selected from halogen, cyano,    hydroxy, oxo, C₁₋₄ alkyl, C₃₋₁₀ cycloalkyl, 3 to 10 membered    heterocyclyl having 1 to 4 heteroatoms independently selected from    nitrogen, oxygen, and sulfur, 6 to 10 membered aryl, 5 to 10    membered heteroaryl having 1 to 4 heteroatoms independently selected    from nitrogen, oxygen, or sulfur, —O—R^(1F1), —N(R^(1F1))(R^(1F2)),    —C(O)N(R^(1F1))(R^(1F2)), —NR^(1F1)C(O)R^(1F2), —S(O)₀₋₂R^(1F1),    —S(O)₂N(R^(1F1))(R^(1F2)), and —NR^(1F1)S(O)₂R^(1F2), wherein each    R^(1F1) and R^(1F2) is independently hydrogen or C₁₋₆ alkyl, wherein    each R^(1E) alkyl, cycloalkyl, aryl, and heteroaryl is optionally    substituted with 1 to 3 R^(1G), which can be the same or different,    and wherein each R^(1G) is independently C₁₋₄ alkyl, C₁₋₄ alkoxy,    hydroxy, halogen, or cyano;-   R² is hydrogen or C₁₋₆ alkyl optionally substituted with 1 to 3    substituents, which can be the same or different, independently    selected from halogen, cyano, C₁₋₄ alkoxy, and C₃₋₁₀ cycloalkyl; or-   R² is C₃₋₆ cycloalkyl optionally substituted with 1 to 3    substituents, which can be the same or different, independently    selected from halogen, cyano, C₁₋₄ alkoxy, and C₁₋₆ alkyl;-   each R³ is independently selected from deuterium, halogen, C₁₋₆    alkyl, C₃₋₆ cycloalkyl, —O—R^(2A1), and —N(R^(2A1))(R^(2A2)),    wherein the C₁₋₆ alkyl is optionally substituted with 1 to 3    substituents, which can be the same or different, independently    selected from C₁₋₄ alkoxy and halogen, and wherein each R^(2A1) and    R^(2A2) is independently hydrogen or C₁₋₃ alkyl optionally    substituted with 1 to 3 halogens, which can be the same or    different;-   n is 0, 1, 2, 3, or 4;-   R⁴ is C₁₋₆ alkyl optionally substituted with 1 to 3 substituents,    which can be the same or different, independently selected from    halogen, cyano, C₁₋₄ alkoxy, —C(O)N(R^(4A1)), and    —N(R^(4A1))(R^(4A2)), wherein each R^(4A1) and R^(4A2) is    independently hydrogen, C₁₋₆ alkyl, or C₃₋₁₀ cycloalkyl; or-   R⁴ is C₃₋₆ cycloalkyl or 3 to 6 membered heterocyclyl having 1 or 2    heteroatoms independently selected from nitrogen, oxygen, and    sulfur, wherein the cycloalkyl or heterocyclyl are optionally    substituted with 1 to 3 substituents, which can be the same or    different, independently selected from halogen, cyano, C₁₋₄ alkyl,    and C₁₋₄ alkoxy;-   each of X¹, X², X³, and X⁴ is independently selected from CH and N;-   each Y¹ and Y² is independently hydrogen, deuterium, or C₁₋₆ alkyl    optionally substituted with 1 to 3 substituents, which can be the    same or different, independently selected from deuterium, halogen,    cyano, C₂₋₃ alkynyl, C₁₋₄ alkoxy, and —C(O)NH—(C₁₋₄H₃₋₉); and-   Z is C₁₋₈ alkyl, C₁₋₆ alkoxy, C₃₋₆ cycloalkyl, C₆₋₁₂ aryl, 3 to 12    membered heterocyclyl having 1 to 4 heteroatoms independently    selected from nitrogen, oxygen, and sulfur, or 5 to 12 membered    heteroaryl having 1 to 4 heteroatoms independently selected from    nitrogen, oxygen, and sulfur, wherein the alkyl, alkoxy, cycloalkyl,    aryl, heterocyclyl, or heteroaryl are each optionally substituted    with 1 to 3 substituents, which can be the same or different,    independently selected from halogen, cyano, C₁₋₄ alkyl, C₁₋₄ alkoxy,    and C₃₋₆ cycloalkyl, wherein the C₁₋₄ alkyl is optionally    substituted with 1 to 3 substituents, which can be the same or    different, selected from C₁₋₄ alkoxy and halogen; or-   Y¹ and Z together with the carbon to which they are attached form    C₃₋₆ cycloalkyl, C₆₋₁₂ aryl, 3 to 12 membered heterocyclyl having 1    to 4 heteroatoms independently selected from nitrogen, oxygen, and    sulfur, or 5 to 12 membered heteroaryl having 1 to 4 heteroatoms    independently selected from nitrogen, oxygen, and sulfur, wherein    the cycloalkyl, aryl, heterocyclyl, or heteroaryl are each    optionally substituted with 1 to 3 substituents, which can be the    same or different, independently selected from cyano, C₁₋₄ alkyl,    C₁₋₄ alkoxy, C₆₋₁₀ aryl, and halogen, wherein the C₁₋₄ alkyl is    optionally substituted with 1 to 3 substituents, which can be the    same or different, independently selected from C₁₋₄ alkoxy and    halogen, and wherein the C₆₋₁₀ aryl is optionally substituted with 1    to 3 substituents, which can be the same or different, independently    selected from C₁₋₄ alkyl, C₁₋₄ alkoxy, and halogen, and Y² is    hydrogen or deuterium.

In some embodiments of the compound of Formula I or pharmaceuticallyacceptable salt thereof

-   R¹ is hydrogen, C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₃₋₁₀    cycloalkyl, 3 to 10 membered heterocyclyl having 1 to 4 heteroatoms    independently selected from nitrogen, oxygen, and sulfur, 6 to 10    membered aryl, or 5 to 10 membered heteroaryl having 1 to 4    heteroatoms independently selected from nitrogen, oxygen, and    sulfur, wherein each alkyl, alkenyl, alkynyl, cycloalkyl,    heterocyclyl, aryl, or heteroaryl is optionally substituted with 1    to 4 R^(1A), which can be the same or different, wherein each R^(1A)    is independently selected from halogen, cyano, oxo, C₁₋₄ alkyl,    C₃₋₁₀ cycloalkyl, 3 to 10 membered heterocyclyl having 1 to 4    heteroatoms independently selected from nitrogen, oxygen, and    sulfur, 6 to 10 membered aryl, 5 to 10 membered heteroaryl having 1    to 4 heteroatoms independently selected from nitrogen, oxygen, or    sulfur, —N(R^(1B1))(R^(1B2)), —O—R^(1B1), —S—R^(1B1),    —C(O)N(R^(1B1))(R^(1B2)), —NR^(1B1)C(O)R^(1B2),    —NR^(1B1)C(O)N(R^(1B2))(R^(1B3)), —S(O)₀₋₂R^(1B1),    —S(O)₂N(R^(1B1))(R^(1B2)), and —NR^(1B1)S(O)₂R^(1B2), wherein each    R^(1B1), R^(1B2), and R^(1B3) is independently hydrogen, or C₁₋₆    alkyl,    -   wherein each R^(1A) alkyl, cycloalkyl, heterocyclyl, aryl, and        heteroaryl is optionally substituted with 1 to 4 R^(1C), which        can be the same or different, and wherein each R^(1C) is        independently C₁₋₄ alkyl, halogen, cyano, —O—R^(1D1),        —N(R^(1D1))(R^(1D2)), and wherein each R^(1D1) and R^(1D2) is        independently hydrogen or C₁₋₆ alkyl; or-   R¹ is —O—R^(1D1) or —N(R^(1D1))(R^(1D2)), wherein each R^(1D1) and    R^(1D2) is independently hydrogen, C₁₋₆ alkyl, or C₃₋₆ cycloalkyl,    wherein each C₁₋₆ alkyl, or C₃₋₆ cycloalkyl is optionally    substituted with 1 to 4 R^(1E), which can be the same or different,    wherein each R^(1E) is independently selected from halogen, cyano,    hydroxy, oxo, C₁₋₄ alkyl, C₃₋₁₀ cycloalkyl, 3 to 10 membered    heterocyclyl having 1 to 4 heteroatoms independently selected from    nitrogen, oxygen, and sulfur, 6 to 10 membered aryl, 5 to 10    membered heteroaryl having 1 to 4 heteroatoms independently selected    from nitrogen, oxygen, or sulfur, —O—R^(1F1), —N(R^(1F1))(R^(1F2)),    —C(O)N(R^(1F1))(R^(1F2)), —NR^(1F1)C(O)R^(1F2), —S(O)₀₋₂R^(1F1),    —S(O)₂N(R^(1F1))(R^(1F2)), and —NR^(1F1)S(O)₂R^(1F2), wherein each    R^(1F1) and R^(1F2) is independently hydrogen or C₁₋₆ alkyl, wherein    each R^(1E) alkyl, cycloalkyl, aryl, and heteroaryl is optionally    substituted with 1 to 3 R^(1G), which can be the same or different,    and wherein each R^(1G) is independently C₁₋₄ alkyl, C₁₋₄ alkoxy,    hydroxy, halogen, or cyano;-   R² is hydrogen or C₁₋₆ alkyl optionally substituted with 1 to 3    substituents, which can be the same or different, independently    selected from halogen, cyano, C₁₋₄ alkoxy, and C₃₋₁₀ cycloalkyl; or-   R² is C₃₋₆ cycloalkyl optionally substituted with 1 to 3    substituents, which can be the same or different, independently    selected from halogen, cyano, C₁₋₄ alkoxy, and C₁₋₆ alkyl;-   each R³ is independently selected from deuterium, halogen, C₁₋₆    alkyl, C₃₋₆ cycloalkyl, —O—R^(2A1), and —N(R^(2A1))(R^(2A2)),    wherein the C₁₋₆ alkyl is optionally substituted with 1 to 3    substituents, which can be the same or different, independently    selected from C₁₋₄ alkoxy and halogen, and wherein each R^(2A1) and    R^(2A2) is independently hydrogen or C₁₋₃ alkyl optionally    substituted with 1 to 3 halogens, which can be the same or    different;-   n is 0, 1, 2, 3, or 4;-   R⁴ is C₁₋₆ alkyl optionally substituted with 1 to 3 substituents,    which can be the same or different, independently selected from    halogen, cyano, C₁₋₄ alkoxy, —C(O)N(R^(4A1)), and    —N(R^(4A1))(R^(4A2)), wherein each R^(4A1) and R^(4A2) is    independently hydrogen, C₁₋₆ alkyl, or C₃₋₁₀ cycloalkyl; or-   R⁴ is C₃₋₆ cycloalkyl or 3 to 6 membered heterocyclyl having 1 or 2    heteroatoms independently selected from nitrogen, oxygen, and    sulfur, wherein the cycloalkyl or heterocyclyl are optionally    substituted with 1 to 3 substituents, which can be the same or    different, independently selected from halogen, cyano, C₁₋₄ alkyl    and C₁₋₄ alkoxy;-   each of X¹, X², X³, and X⁴ is independently selected from CH and N;-   each Y¹ and Y² is independently hydrogen, deuterium, or C₁₋₆ alkyl    optionally substituted with 1 to 3 substituents, which can be the    same or different, independently selected from deuterium, halogen,    cyano, C₂₋₃ alkynyl, C₁₋₄ alkoxy, and —C(O)NH—(C₁₋₄H₃₋₉); and-   Z is C₁₋₈ alkyl, C₁₋₆ alkoxy, C₃₋₆ cycloalkyl, C₆₋₁₂ aryl, 3 to 12    membered heterocyclyl having 1 to 4 heteroatoms independently    selected from nitrogen, oxygen, and sulfur, or 5 to 12 membered    heteroaryl having 1 to 4 heteroatoms independently selected from    nitrogen, oxygen, and sulfur, wherein the alkyl, alkoxy, cycloalkyl,    aryl, heterocyclyl, or heteroaryl are each optionally substituted    with 1 to 3 substituents, which can be the same or different,    independently selected from halogen, cyano, C₁₋₄ alkyl, C₁₋₄ alkoxy,    and C₃₋₆ cycloalkyl, wherein the C₁₋₄ alkyl is optionally    substituted with 1 to 3 substituents, which can be the same or    different, selected from C₁₋₄ alkoxy and halogen; or-   Y¹ and Z together with the carbon to which they are attached form    C₃₋₆ cycloalkyl, C₆₋₁₂ aryl, 3 to 12 membered heterocyclyl having 1    to 4 heteroatoms independently selected from nitrogen, oxygen, and    sulfur, or 5 to 12 membered heteroaryl having 1 to 4 heteroatoms    independently selected from nitrogen, oxygen, and sulfur, wherein    the cycloalkyl, aryl, heterocyclyl, or heteroaryl are each    optionally substituted with 1 to 3 substituents, which can be the    same or different, independently selected from cyano, C₁₋₄ alkyl,    C₁₋₄ alkoxy, C₆₋₁₀ aryl, and halogen, wherein the C₁₋₄ alkyl is    optionally substituted with 1 to 3 substituents, which can be the    same or different, independently selected from C₁₋₄ alkoxy and    halogen, and wherein the C₆₋₁₀ aryl is optionally substituted with 1    to 3 substituents, which can be the same or different, independently    selected from C₁₋₄ alkyl, C₁₋₄ alkoxy, and halogen, and Y² is    hydrogen or deuterium.

In some embodiments, provided herein are pharmaceutical compositionscomprising a compound provided herein, or pharmaceutically acceptablesalt thereof, and a pharmaceutically acceptable excipient or carrier. Insome embodiments, the pharmaceutical compositions comprise atherapeutically effective amount of a compound provided herein, orpharmaceutically acceptable salt thereof, and a pharmaceuticallyacceptable excipient or carrier.

In some embodiments, the pharmaceutical compositions provided hereinfurther comprise one or more (e.g., one, two, three, four, one or two,one to three, or one to four) additional therapeutic agents, orpharmaceutically acceptable salts thereof. In some embodiments, thepharmaceutical compositions further comprise a therapeutically effectiveamount of the one or more (e.g., one, two, three, four, one or two, oneto three, or one to four) additional therapeutic agents, orpharmaceutically acceptable salts thereof.

In some embodiments, the present disclosure provides methods ofinhibiting LPAR1 activity in a subject in need thereof, comprisingadministering to the subject a therapeutically effective amount of acompound provided herein (e.g., a compound of Formula (I), (Ia), (IIa),(IIb), (IIc), (IId), (IIe), (IIf), (IIg), (IIh), or (IIi)), orpharmaceutically acceptable salt thereof, or a pharmaceuticalcomposition provided herein.

In some embodiments, the present disclosure provides methods of treatinga patient having an LPAR1 mediated condition, comprising administeringto the patient a therapeutically effective amount of a compound providedherein (e.g., a compound of Formula (I), (Ia), (IIa), (IIa), (IIc),(IId), (IIe), (IIf), (IIg), (IIh), or (Ili)), or pharmaceuticallyacceptable salt thereof, or a pharmaceutical composition providedherein.

DETAILED DESCRIPTION

The present disclosure relates to LPA receptor antagonists, such asantagonists of LPAR1. The disclosure also relates to compositions andmethods relating to LPAR1 antagonists and the use of such compounds fortreatment and/or prophylaxis of LPAR1-mediated diseases and conditions.The disclosure also relates to compositions and methods of treatingand/or preventing liver disease including an LPAR1 antagonist incombination with one or more additional therapeutic agents.

It is commonly believed that patients with certain LPAR1-mediateddiseases, such as cancer, fibrosis, inflammation, pain, andcardiovascular diseases, or liver diseases including non-alcoholic fattyliver disease (NAFLD) and non-alcoholic steatohepatitis (NASH) canbenefit from the treatment with an LPAR1 antagonist and optionally oneor more additional therapeutic agents.

Definitions and General Parameters

The description below is made with the understanding that the presentdisclosure is to be considered as an exemplification of the claimedsubject matter and is not intended to limit the appended claims to thespecific embodiments illustrated. The headings used throughout thisdisclosure are provided for convenience and are not to be construed tolimit the claims in any way. Embodiments illustrated under any headingmay be combined with embodiments illustrated under any other heading.

Unless defined otherwise, all technical and scientific terms used hereinhave the same meaning as commonly understood by one of ordinary skill inthe art. It must be noted that as used herein and in the appendedclaims, the singular forms “a”, “and”, and “the” include pluralreferents unless the context clearly dictates otherwise. Thus, e.g.,reference to “the compound” includes a plurality of such compounds andreference to “the assay” includes reference to one or more assays andequivalents thereof known to those skilled in the art, and so forth.

As used in the present specification, the following terms and phrasesare generally intended to have the meanings as set forth below, exceptto the extent that the context in which they are used indicatesotherwise.

A dash (“-”) that is not between two letters or symbols is used toindicate a point of attachment for a substituent. For example, —CONH₂ isattached through the carbon atom. A dash at the front or end of achemical group is a matter of convenience; chemical groups may bedepicted with or without one or more dashes without losing theirordinary meaning. A wavy line drawn through a line in a structureindicates a point of attachment of a group. Unless chemically orstructurally required, no directionality is indicated or implied by theorder in which a chemical group is written or named. A solid line comingout of the center of a ring indicates that the point of attachment for asubstituent on the ring can be at any ring atom. For example, R^(a) inthe below structure can be attached to any of the five carbon ring atomsor R^(a) can replace the hydrogen attached to the nitrogen ring atom:

The prefix “C_(u-v)” indicates that the following group has from u to vcarbon atoms. For example, “C₁₋₆ alkyl” indicates that the alkyl grouphas from 1 to 6 carbon atoms. Likewise, the term “x-y membered” rings,wherein x and y are numerical ranges, such as “3 to 12-memberedheterocyclyl”, refers to a ring containing x-y atoms (e.g., 3-12), ofwhich up to 80% may be heteroatoms, such as N, O, S, P, and theremaining atoms are carbon.

Also, certain commonly used alternative chemical names may or may not beused. For example, a divalent group such as a divalent “alkyl” group, adivalent “aryl” group, etc., may also be referred to as an “alkylene”group or an “alkylenyl” group, or alkylyl group, an “arylene” group oran “arylenyl” group, or arylyl group, respectively.

“A compound disclosed herein” or “a compound of the present disclosure”or “a compound provided herein” or “a compound described herein” refersto the compounds of Formula (I), (Ia), (IIa), (IIb), (IIc), (IId),(IIe), (IIf), (IIg), (IIh), or (IIi). Also included are the specificCompounds 1 to 338 provided herein (e.g., Examples 1-92).

Reference to “about” a value or parameter herein includes (anddescribes) embodiments that are directed to that value or parameter perse. In certain embodiments, the term “about” includes the indicatedamount±10%. In other embodiments, the term “about” includes theindicated amount±5%. In certain other embodiments, the term “about”includes the indicated amount±1%. Also, to the term “about X” includesdescription of “X”. Also, the singular forms “a” and “the” includeplural references unless the context clearly dictates otherwise. Thus,e.g., reference to “the compound” includes a plurality of such compoundsand reference to “the assay” includes reference to one or more assaysand equivalents thereof known to those skilled in the art.

“Alkyl” refers to an unbranched or branched saturated hydrocarbon chain.As used herein, alkyl has 1 to 20 carbon atoms (i.e., C₁₋₂₀ alkyl), 1 to8 carbon atoms (i.e., C₁₋₈ alkyl), 1 to 6 carbon atoms (i.e., C₁₋₆alkyl), 1 to 4 carbon atoms (i.e., C₁₋₄ alkyl), or 1 to 3 carbon atoms(i.e., C₁₋₃ alkyl). Examples of alkyl groups include methyl, ethyl,propyl, isopropyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, pentyl,2-pentyl, isopentyl, neopentyl, hexyl, 2-hexyl, 3-hexyl, and3-methylpentyl. When an alkyl residue having a specific number ofcarbons is named by chemical name or identified by molecular formula,all positional isomers having that number of carbons may be encompassed;thus, for example, “butyl” includes n-butyl (i.e., —(CH₂)₃CH₃),sec-butyl (i.e., —CH(CH₃)CH₂CH₃), isobutyl (i.e., —CH₂CH(CH₃)₂) andtert-butyl (i.e., —C(CH₃)₃); and “propyl” includes n-propyl (i.e.,—(CH₂)₂CH₃) and isopropyl (i.e., —CH(CH₃)₂).

“Alkenyl” refers to an aliphatic group containing at least onecarbon-carbon double bond and having from 2 to 20 carbon atoms (i.e.,C₂₋₂₀ alkenyl), 2 to 8 carbon atoms (i.e., C₂₋₈ alkenyl), 2 to 6 carbonatoms (i.e., C₂₋₆ alkenyl), or 2 to 4 carbon atoms (i.e., C₂₋₄ alkenyl).Examples of alkenyl groups include ethenyl, propenyl, butadienyl(including 1,2-butadienyl and 1,3-butadienyl).

“Alkynyl” refers to an aliphatic group containing at least onecarbon-carbon triple bond and having from 2 to 20 carbon atoms (i.e.,C₂₋₂₀ alkynyl), 2 to 8 carbon atoms (i.e., C₂₋₈ alkynyl), 2 to 6 carbonatoms (i.e., C₂₋₆ alkynyl), or 2 to 4 carbon atoms (i.e., C₂₋₄ alkynyl).The term “alkynyl” also includes those groups having one triple bond andone double bond.

“Alkoxy” refers to the group “alkyl-O—”. Examples of alkoxy groupsinclude methoxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, tert-butoxy,sec-butoxy, n-pentoxy, n-hexoxy, and 1,2-dimethylbutoxy.

“Acyl” refers to a group —C(═O)R, wherein R is hydrogen, alkyl,cycloalkyl, heterocyclyl, aryl, heteroalkyl, or heteroaryl; each ofwhich may be optionally substituted, as defined herein. Examples of acylinclude formyl, acetyl, cylcohexylcarbonyl, cyclohexylmethylcarbonyl,and benzoyl.

“Amino” refers to the group —NR^(y)R^(z) wherein R^(y) and R^(z) areindependently selected from the group consisting of hydrogen, alkyl,haloalkyl, aryl, heteroaryl, cycloalkyl, or heterocyclyl; each of whichmay be optionally substituted.

“Aryl” refers to an aromatic carbocyclic group having a single ring(e.g., monocyclic) or multiple rings (e.g., bicyclic or tricyclic)including fused systems. As used herein, aryl has 6 to 20 ring carbonatoms (i.e., C₆₋₂₀ aryl), 6 to 12 carbon ring atoms (i.e., C₆₋₁₂ aryl),or 6 to 10 carbon ring atoms (i.e., C₆₋₁₀ aryl). Examples of aryl groupsinclude phenyl, naphthyl, fluorenyl, and anthryl. Aryl, however, doesnot encompass or overlap in any way with heteroaryl defined below. Ifone or more aryl groups are fused with a heteroaryl ring, the resultingring system is heteroaryl.

“Cyano” or “carbonitrile” refers to the group —CN.

“Cycloalkyl” refers to a saturated or partially saturated cyclic alkylgroup having a single ring or multiple rings including fused, bridged,and spiro ring systems. The term “cycloalkyl” includes cycloalkenylgroups (i.e., the cyclic group having at least one double bond). As usedherein, cycloalkyl has from 3 to 20 ring carbon atoms (i.e., C₃₋₂₀cycloalkyl), 3 to 12 ring carbon atoms (i.e., C₃₋₁₂ cycloalkyl), 3 to 10ring carbon atoms (i.e., C₃₋₁₀ cycloalkyl), 3 to 8 ring carbon atoms(i.e., C₃₋₈ cycloalkyl), or 3 to 6 ring carbon atoms (i.e., C₃₋₆cycloalkyl). Examples of cycloalkyl groups include cyclopropyl,cyclobutyl, cyclopentyl, and cyclohexyl.

“Fused” refers to a ring which is bound to an adjacent ring. In someembodiments the fused ring system is a heterocyclyl. In some embodimentsthe fused ring system is a oxabicyclohexanyl. In some embodiments thefused ring system is

“Bridged” refers to a ring fusion wherein non-adjacent atoms on a ringare joined by a divalent substituent, such as alkylenyl group, analkylenyl group containing one or two heteroatoms, or a singleheteroatom. Quinuclidinyl and admantanyl are examples of bridged ringsystems. In some embodiments the bridged ring is a bicyclopentanyl(bicycle[1.1.1]pentanyl) or bicyclooctanyl (bicycle[2.2.2]octanyl). Insome embodiments, the bridge ring is

“Spiro” refers to a ring substituent which is joined by two bonds at thesame carbon atom. Examples of spiro groups include1,1-diethylcyclopentane, dimethyl-dioxolane, and4-benzyl-4-methylpiperidine, wherein the cyclopentane and piperidine,respectively, are the spiro substituents. In some embodiments the spirosubstituent is a spiropentanyl (spiro[a.b]pentanyl), spirohexanyl,spiroheptanyl, or spirodecanyl. In some embodiments the spirosubstituent is

“Halogen” or “halo” includes fluoro, chloro, bromo, and iodo.

“Heteroaryl” refers to an aromatic group having a single ring, multiplerings, or multiple fused rings, with one or more ring heteroatomsindependently selected from nitrogen, oxygen, and sulfur. As usedherein, heteroaryl includes 1 to 20 carbon ring atoms (i.e., C₁₋₂₀heteroaryl), 3 to 12 carbon ring atoms (i.e., C₃₋₁₂ heteroaryl), or 3 to8 carbon ring atoms (i.e., C₃₋₈ heteroaryl); and 1 to 5 ringheteroatoms, 1 to 4 ring heteroatoms, 1 to 3 ring heteroatoms, 1 to 2ring heteroatoms, or 1 ring heteroatom independently selected fromnitrogen, oxygen, and sulfur. Examples of heteroaryl groups includepyrimidinyl, purinyl, pyridyl, pyridazinyl, benzothiazolyl, andpyrazolyl. Heteroaryl does not encompass or overlap with aryl as definedabove.

“Heterocyclyl” or “heterocyclic ring” or “heterocycle” refers to anon-aromatic cyclic alkyl group, with one or more ring heteroatomsindependently selected from nitrogen, oxygen and sulfur. As used herein,“heterocyclyl” or “heterocyclic ring” or “heterocycle” refer to ringsthat are saturated or partially saturated unless otherwise indicated,e.g., in some embodiments “heterocyclyl” or “heterocyclic ring” or“heterocycle” refers to rings that are partially saturated wherespecified. The term “heterocyclyl” or “heterocyclic ring” or“heterocycle” includes heterocycloalkenyl groups (i.e., the heterocyclylgroup having at least one double bond). A heterocyclyl may be a singlering or multiple rings wherein the multiple rings may be fused, bridged,or spiro. As used herein, heterocyclyl has 2 to 20 carbon ring atoms(i.e., C₂₋₂₀ heterocyclyl), 2 to 12 carbon ring atoms (i.e., C₂₋₁₂heterocyclyl), 2 to 10 carbon ring atoms (i.e., C₂₋₁₀ heterocyclyl), 2to 8 carbon ring atoms (i.e., C₂₋₈ heterocyclyl), 3 to 12 carbon ringatoms (i.e., C₃₋₁₂ heterocyclyl), 3 to 8 carbon ring atoms (i.e., C₃₋₈heterocyclyl), or 3 to 6 carbon ring atoms (i.e., C₃₋₆ heterocyclyl);having 1 to 5 ring heteroatoms, 1 to 4 ring heteroatoms, 1 to 3 ringheteroatoms, 1 to 2 ring heteroatoms, or 1 ring heteroatom independentlyselected from nitrogen, sulfur or oxygen. Examples of heterocyclylgroups include pyrrolidinyl, piperidinyl, piperazinyl, oxetanyl,dioxolanyl, azetidinyl, and morpholinyl. As used herein, the terms“heterocycle”, “heterocyclyl”, and “heterocyclic ring” are usedinterchangeably.

“Hydroxy” or “hydroxyl” refers to the group —OH.

“Oxo” refers to the group (═O) or (O).

“Sulfonyl” refers to the group —S(O)₂R^(c), where R^(c) is alkyl,heterocyclyl, cycloalkyl, heteroaryl, or aryl. Examples of sulfonyl aremethylsulfonyl, ethylsulfonyl, phenylsulfonyl, and toluenesulfonyl.

Whenever the graphical representation of a group terminates in a singlybonded nitrogen atom, that group represents an —NH₂ group unlessotherwise indicated. Similarly, unless otherwise expressed, hydrogenatom(s) are implied and deemed present where necessary in view of theknowledge of one of skill in the art to complete valency or providestability.

The terms “optional” or “optionally” mean that the subsequentlydescribed event or circumstance may or may not occur, and that thedescription includes instances where said event or circumstance occursand instances in which it does not. Also, the term “optionallysubstituted” means that any one or more hydrogen atoms on the designatedatom or group may or may not be replaced by a moiety other thanhydrogen.

The term “substituted” means that any one or more hydrogen atoms on thedesignated atom or group is replaced with one or more substituents otherthan hydrogen, provided that the designated atom's normal valence is notexceeded. The one or more substituents include, but are not limited to,alkyl, alkenyl, alkynyl, alkoxy, acyl, amino, amido, amidino, aryl,azido, carbamoyl, carboxyl, carboxyl ester, cyano, guanidino, halo,haloalkyl, heteroalkyl, heteroaryl, heterocyclyl, hydroxy, hydrazino,imino, oxo, nitro, alkylsulfinyl, sulfonic acid, alkylsulfonyl,thiocyanate, thiol, thione, or combinations thereof. Polymers or similarindefinite structures arrived at by defining substituents with furthersubstituents appended ad infinitum (e.g., a substituted aryl having asubstituted alkyl which is itself substituted with a substituted arylgroup, which is further substituted by a substituted heteroalkyl group,etc.) are not intended for inclusion herein. Unless otherwise noted, themaximum number of serial substitutions in compounds described herein isthree. For example, serial substitutions of substituted aryl groups withtwo other substituted aryl groups are limited to ((substitutedaryl)substituted aryl) substituted aryl. Similarly, the abovedefinitions are not intended to include impermissible substitutionpatterns (e.g., methyl substituted with 5 fluorines or heteroaryl groupshaving two adjacent oxygen ring atoms). Such impermissible substitutionpatterns are well known to the skilled artisan. When used to modify achemical group, the term “substituted” may describe other chemicalgroups defined herein. For example, the term “substituted aryl”includes, but is not limited to, “alkylaryl.” Unless specifiedotherwise, where a group is described as optionally substituted, anysubstituents of the group are themselves unsubstituted.

In some embodiments, the term “substituted alkyl” refers to an alkylgroup having one or more substituents including hydroxyl, halo, amino,alkoxy, cycloalkyl, heterocyclyl, aryl, and heteroaryl. In additionalembodiments, “substituted cycloalkyl” refers to a cycloalkyl grouphaving one or more substituents including alkyl, haloalkyl, cycloalkyl,heterocyclyl, aryl, heteroaryl, amino, alkoxy, halo, oxo, and hydroxyl;“substituted heterocyclyl” refers to a heterocyclyl group having one ormore substituents including alkyl, amino, haloalkyl, heterocyclyl,cycloalkyl, aryl, heteroaryl, alkoxy, halo, oxo, and hydroxyl;“substituted aryl” refers to an aryl group having one or moresubstituents including halo, alkyl, amino, haloalkyl, cycloalkyl,heterocyclyl, heteroaryl, alkoxy, and cyano; “substituted heteroaryl”refers to an heteroaryl group having one or more substituents includinghalo, amino, alkyl, haloalkyl, cycloalkyl, aryl, heterocyclyl,heteroaryl, alkoxy, and cyano and “substituted sulfonyl” refers to agroup —S(O)₂R, in which R is substituted with one or more substituentsincluding alkyl, cycloalkyl, heterocyclyl, aryl, and heteroaryl. Inother embodiments, the one or more substituents may be furthersubstituted with halo, alkyl, haloalkyl, hydroxyl, alkoxy, cycloalkyl,heterocyclyl, aryl, or heteroaryl, each of which is substituted. Inother embodiments, the substituents may be further substituted withhalo, alkyl, haloalkyl, alkoxy, hydroxyl, cycloalkyl, heterocyclyl,aryl, or heteroaryl, each of which is unsubstituted.

In some embodiments, a substituted cycloalkyl, a substitutedheterocyclyl, a substituted aryl, and/or a substituted heteroarylincludes a cycloalkyl, a heterocyclyl, an aryl, and/or a heteroaryl thathas a substituent on the ring atom to which the cycloalkyl,heterocyclyl, aryl, and/or heteroaryl is attached to the rest of thecompound. For example, in the below moiety, the cyclopropyl issubstituted with a methyl group:

The disclosures illustratively described herein may suitably bepracticed in the absence of any element or elements, limitation orlimitations, not specifically disclosed herein. Thus, for example, theterms “comprising,” “including,” “containing,” etc., shall be readexpansively and without limitation. Additionally, the terms andexpressions employed herein have been used as terms of description andnot of limitation, and there is no intention in the use of such termsand expressions of excluding any equivalents of the features shown anddescribed or portions thereof, but it is recognized that variousmodifications are possible within the scope of the disclosure claimed.

The compounds of the present disclosure can be in the form of apharmaceutically acceptable salt. The term “pharmaceutically acceptablesalts” refers to salts prepared from pharmaceutically acceptablenon-toxic bases or acids, including inorganic bases or acids and organicbases or acids. The compounds of the present disclosure can be in theform of a pharmaceutically acceptable salt. The term “pharmaceuticallyacceptable salts” refers to salts prepared from pharmaceuticallyacceptable non-toxic bases or acids, including inorganic bases or acidsand organic bases or acids. In case the compounds of the presentdisclosure contain one or more acidic or basic groups, the disclosurealso comprises their corresponding pharmaceutically or toxicologicallyacceptable salts, in particular their pharmaceutically utilizable salts.Thus, the compounds of the present disclosure which contain acidicgroups can be present on these groups and can be used according to thedisclosure, for example, as alkali metal salts, alkaline earth metalsalts or ammonium salts. More precise examples of such salts includesodium salts, potassium salts, calcium salts, magnesium salts or saltswith ammonia or organic amines such as, for example, ethylamine,ethanolamine, triethanolamine, amino acids, or other bases known topersons skilled in the art. The compounds of the present disclosurewhich contain one or more basic groups, i.e., groups which can beprotonated, can be present and can be used according to the disclosurein the form of their addition salts with inorganic or organic acids.Examples of suitable acids include hydrogen chloride, hydrogen bromide,phosphoric acid, sulfuric acid, nitric acid, methanesulfonic acid,p-toluenesulfonic acid, naphthalenedisulfonic acids, oxalic acid, aceticacid, tartaric acid, lactic acid, salicylic acid, benzoic acid, formicacid, propionic acid, pivalic acid, diethylacetic acid, malonic acid,succinic acid, pimelic acid, fumaric acid, maleic acid, malic acid,sulfaminic acid, phenylpropionic acid, gluconic acid, ascorbic acid,isonicotinic acid, citric acid, adipic acid, and other acids known topersons skilled in the art.

If the compounds of the present disclosure simultaneously contain acidicand basic groups in the molecule, the disclosure also includes, inaddition to the salt forms mentioned, inner salts or betaines(zwitterions). The respective salts can be obtained by customary methodswhich are known to the person skilled in the art like, for example, bycontacting these with an organic or inorganic acid or base in a solventor dispersant, or by anion exchange or cation exchange with other salts.

The present disclosure also includes all salts of the compounds of thepresent disclosure which, owing to low physiological compatibility, arenot directly suitable for use in pharmaceuticals but which can be used,for example, as intermediates for chemical reactions or for thepreparation of pharmaceutically acceptable salts. Acids and bases usefulfor reaction with an underlying compound to form pharmaceuticallyacceptable salts (acid addition or base addition salts respectively) areknown to one of skill in the art. Similarly, methods of preparingpharmaceutically acceptable salts from an underlying compound (upondisclosure) are known to one of skill in the art and are disclosed infor example, Berge, at al. Journal of Pharmaceutical Science, January1977 vol. 66, No. 1, and other sources.

Furthermore, compounds disclosed herein may be subject to tautomerism.Where tautomerism, e.g., keto-enol tautomerism, of compounds or theirprodrugs may occur, the individual forms, like, e.g., the keto and enolform, are each within the scope of the disclosure as well as theirmixtures in any ratio. The same applies for stereoisomers, like, e.g.,enantiomers, cis/trans isomers, diastereomers, conformers, and the like.

The term “protecting group” refers to a moiety of a compound that masksor alters the properties of a functional group or the properties of thecompound as a whole. Chemical protecting groups and strategies forprotection/deprotection are well known in the art. See e.g., ProtectiveGroups in Organic Chemistry, Theodora W. Greene, John Wiley & Sons,Inc., New York, 1991. Protecting groups are often utilized to mask thereactivity of certain functional groups, to assist in the efficiency ofdesired chemical reactions, e.g., making and breaking chemical bonds inan ordered and planned fashion. The term “deprotecting” refers toremoving the protecting group.

It will be appreciated by the skilled person that when lists ofalternative substituents include members which, because of their valencyrequirements or other reasons, cannot be used to substitute a particulargroup, the list is intended to be read with the knowledge of the skilledperson to include only those members of the list which are suitable forsubstituting the particular group.

Further the compounds of the present disclosure may be present in theform of solvates, such as those which include as solvate water, orpharmaceutically acceptable solvates, such as alcohols, in particularethanol. A “solvate” is formed by the interaction of a solvent and acompound.

In certain embodiments, provided are optical isomers, racemates, orother mixtures thereof of the compounds described herein or apharmaceutically acceptable salt or a mixture thereof If desired,isomers can be separated by methods well known in the art, e.g., byliquid chromatography. In those situations, the single enantiomer ordiastereomer, i.e., optically active form, can be obtained by asymmetricsynthesis or by resolution. Resolution can be accomplished, for example,by conventional methods such as crystallization in the presence of aresolving agent, or chromatography, using for example, a chiralhigh-pressure liquid chromatography (HPLC) column.

A “stereoisomer” refers to a compound made up of the same atoms bondedby the same bonds but having different three-dimensional structures,which are not interchangeable. The present invention contemplatesvarious stereoisomers and mixtures thereof and includes “enantiomers,”which refers to two stereoisomers whose molecules are nonsuperimposeablemirror images of one another. “Diastereomers” are stereoisomers thathave at least two asymmetric atoms, but which are not mirror-images ofeach other.

Compounds disclosed herein and their pharmaceutically acceptable saltsmay, in some embodiments, include an asymmetric center and may thus giverise to enantiomers, diastereomers, and other stereoisomeric forms thatmay be defined, in terms of absolute stereochemistry, as (R)- or (S)-or, as (D)- or (L)- for amino acids. Some embodiments include all suchpossible isomers, as well as their racemic and optically pure forms.Optically active (+) and (−), (R)- and (S)-, or (D)- and (L)-isomers maybe prepared using chiral synthons or chiral reagents, or resolved usingconventional techniques, for example, chromatography and fractionalcrystallization. Conventional techniques for the preparation/isolationof individual enantiomers include chiral synthesis from a suitableoptically pure precursor or resolution of the racemate (or the racemateof a salt or derivative) using, for example, chiral high-pressure liquidchromatography (HPLC). When the compounds described herein containolefinic double bonds or other centres of geometric asymmetry, andunless specified otherwise, it is intended that the compounds includeboth E and Z geometric isomers.

Compositions provided herein that include a compound described herein orpharmaceutically acceptable salts, isomer, or a mixture thereof mayinclude racemic mixtures, or mixtures containing an enantiomeric excessof one enantiomer or single diastereomers or diastereomeric mixtures.All such isomeric forms of these compounds are expressly included hereinthe same as if each and every isomeric form were specifically andindividually listed.

Any formula or structure given herein is also intended to representunlabeled forms as well as isotopically labeled forms of the compounds.Isotopically labeled compounds have structures depicted by the formulasgiven herein except that one or more atoms are replaced by an atomhaving a selected atomic mass or mass number. Examples of isotopes thatcan be incorporated into compounds of the disclosure include isotopes ofhydrogen, carbon, nitrogen, oxygen, phosphoros, fluorine and chlorine,such as, but not limited to ²H (deuterium, D), ³H (tritium), ¹¹C, ¹³C,¹⁴C, ¹⁵N, ¹⁸F, ³¹P, ³²P, ³⁵S, ³⁶Cl and ¹²⁵I. Various isotopicallylabeled compounds of the present disclosure, for example those intowhich radioactive isotopes such as ³H, ¹³C and ¹⁴C are incorporated.Such isotopically labelled compounds may be useful in metabolic studies,reaction kinetic studies, detection or imaging techniques, such aspositron emission tomography (PET) or single-photon emission computedtomography (SPECT) including drug or substrate tissue distributionassays or in radioactive treatment of patients. Isotopically labeledcompounds of this disclosure and prodrugs thereof can generally beprepared by carrying out the procedures disclosed in the schemes or inthe examples and preparations described below by substituting a readilyavailable isotopically labeled reagent for a non-isotopically labeledreagent.

The disclosure also includes “deuterated analogs” of compounds disclosedherein, in which from 1 to n hydrogens attached to a carbon atom is/arereplaced by deuterium, in which n is the number of hydrogens in themolecule. Such compounds may exhibit increased resistance to metabolismand thus be useful for increasing the half-life of any compound ofFormula (I) when administered to a mammal, e.g., a human. See, e.g.,Foster, “Deuterium Isotope Effects in Studies of Drug Metabolism,”Trends Pharmacol. Sci. 5(12):524-527 (1984). Such compounds aresynthesized by means well known in the art, for example by employingstarting materials in which one or more hydrogens have been replaced bydeuterium.

Deuterium labelled or substituted therapeutic compounds of thedisclosure may have beneficial DMPK (drug metabolism andpharmacokinetics) properties, relating to distribution, metabolism andexcretion (ADME). Substitution with heavier isotopes such as deuteriummay afford certain therapeutic advantages resulting from greatermetabolic stability, for example increased in vivo half-life, reduceddosage requirements and/or an improvement in therapeutic index. An ¹⁸Flabeled compound may be useful for PET or SPECT studies.

The concentration of such a heavier isotope, specifically deuterium, maybe defined by an isotopic enrichment factor. In the compounds of thisdisclosure any atom not specifically designated as a particular isotopeis meant to represent any stable isotope of that atom. Unless otherwisestated, when a position is designated specifically as “H” or “hydrogen”,the position is understood to have hydrogen at its natural abundanceisotopic composition. Accordingly, in the compounds of this disclosureany atom specifically designated as a deuterium (D) is meant torepresent deuterium.

Furthermore, the present disclosure provides pharmaceutical compositionscomprising a compound of the present disclosure, or a prodrug compoundthereof, or a pharmaceutically acceptable salt or solvate thereof asactive ingredient together with a pharmaceutically acceptable carrier.

“Pharmaceutical composition” means one or more active ingredients, andone or more inert ingredients that make up the carrier, as well as anyproduct which results, directly or indirectly, from combination,complexation or aggregation of any two or more of the ingredients, orfrom dissociation of one or more of the ingredients, or from other typesof reactions or interactions of one or more of the ingredients.Accordingly, the pharmaceutical compositions of the present disclosurecan encompass any composition made by admixing at least one compound ofthe present disclosure and a pharmaceutically acceptable carrier.

As used herein, “pharmaceutically acceptable carrier” includesexcipients or agents such as solvents, diluents, dispersion media,coatings, antibacterial and antifungal agents, isotonic and absorptiondelaying agents and the like that are not deleterious to the disclosedcompound or use thereof. The use of such carriers and agents to preparecompositions of pharmaceutically active substances is well known in theart (see, e.g., Remington's Pharmaceutical Sciences, Mace PublishingCo., Philadelphia, Pa. 17th Ed. (1985); and Modern Pharmaceutics, MarcelDekker, Inc. 3rd Ed. (G.S. Banker & C.T. Rhodes, Eds.).

“IC₅₀” or “EC₅₀” refers to the inhibitory concentration required toachieve 50% of the maximum desired effect. In many cases here themaximum desired effect is the inhibition of LPA induced LPAR1activation. This term is obtained using an in vitro assay, such as acalcium mobilization assay, evaluating the concentration-dependentinhibition of LPA induced LPAR1 activity.

“Treatment” or “treating” is an approach for obtaining beneficial ordesired results including clinical results. Beneficial or desiredclinical results may include one or more of the following: a) inhibitingthe disease or condition (e.g., decreasing one or more symptomsresulting from the disease or condition, and/or diminishing the extentof the disease or condition); b) slowing or arresting the development ofone or more clinical symptoms associated with the disease or condition(e.g., stabilizing the disease or condition, preventing or delaying theworsening or progression of the disease or condition, and/or preventingor delaying the spread (e.g., metastasis) of the disease or condition);and/or c) relieving the disease, that is, causing the regression ofclinical symptoms (e.g., ameliorating the disease state, providingpartial or total remission of the disease or condition, enhancing effectof another medication, delaying the progression of the disease,increasing the quality of life, and/or prolonging survival. In someembodiments, the term “treatment” or “treating” means administering acompound or pharmaceutically acceptable salt of Formula (I), (Ia),(IIa), (IIb), (IIc), (IId), (IIe), (IIf), (IIg), (IIh), or (IIi) for thepurpose of: (i) delaying the onset of a disease, that is, causing theclinical symptoms of the disease not to develop or delaying thedevelopment thereof; (ii) inhibiting the disease, that is, arresting thedevelopment of clinical symptoms; and/or (iii) relieving the disease,that is, causing the regression of clinical symptoms or the severitythereof.

“Prevention” or “preventing” means any treatment of a disease orcondition that causes the clinical symptoms of the disease or conditionnot to develop. Compounds may, in some embodiments, be administered to asubject (including a human) who is at risk or has a family history ofthe disease or condition.

“Subject” refers to an animal, such as a mammal (including a human),that has been or will be the object of treatment, observation orexperiment. The methods described herein may be useful in human therapyand/or veterinary applications. In some embodiments, the subject is amammal. In some embodiments, the subject is a human.

The term “therapeutically effective amount” or “effective amount” of acompound described herein or a pharmaceutically acceptable salt,tautomer, stereoisomer, mixture of stereoisomers, prodrug, or deuteratedanalog thereof means an amount sufficient to effect treatment whenadministered to a subject, to provide a therapeutic benefit such asamelioration of symptoms or slowing of disease progression. For example,a therapeutically effective amount may be an amount sufficient todecrease a symptom of a disease or condition responsive to LPAR1antagonists. The therapeutically effective amount may vary depending onthe subject, and disease or condition being treated, the weight and ageof the subject, the severity of the disease or condition, and the mannerof administering, which can readily be determined by one or ordinaryskill in the art.

List of Abbreviations and Acronyms Abbreviation Meaning ACN or MeCNAcetonitrile aq. Aqueous Bn Benzyl COPD Chronic Obstructive PulmonaryDisease DCM Dichloromethane DIEA N,N-Diisopropylethylamine DMFN,N-Dimethylformamide DMSO Dimethylsulfoxide DPPA Diphenylphosphorylazide EA Ethyl acetate EDTA Ethylenediaminetetraacetic acid ESIElectronspray Ionization Et Ethyl Et₂O Diethyl ether EtOAc Ethyl acetateh or hr(s) Hour(s) HBSS Hanks’ Balanced Salt solution HCC Hepatocellularcarcinoma HPLC High performance liquid chromatography LCMS or LiquidChromatography Mass Spectrometry LC/MS LPA Lysophosphatidic acid LPCLysophosphatidylcholine Me Methyl MeOH Methanol MS Mass Spectrometry m/zMass-to-charge ratio NADPH Dihydronicotinamide-adenine dinucleotidephosphate NAFLD Non-alcoholic fattyl liver disease NASH Non-alcoholicsteatohepatitis NMR Nuclear Magnetic Resonance spectroscopy PBC PrimaryBiliary Cirrhosis PE Petroleum ether PSC Primary Sclerosing Choleangitisrpm Revolutions per minute RT or rt Room temperature sat. SaturatedTEMPO 2,2,6,6-Tetramethylpiperidine 1-oxyl TFA Trifluoroacetic acid THFTetrahydrofuran T3P Propanephosphonic acid anhydride

As used herein, an “LPAR1 antagonist” refers to any agent that iscapable of binding and inhibiting LPAR1. LPAR1, also known as LPA₁, is aGPCR that binds the lipid signaling molecule lysophosphatidic acid(LPA). Exemplary reference sequences for LPAR1 include the NCBIReference Sequences NP_001392 (human protein), NP_001277415 (mouseprotein), NM_001401 (human mRNA), and NM_001290486 (mouse mRNA). LPAR1antagonists can act as competitive inhibitors of full or partial LPAR1agonists, or as inverse agonists. The activity of an LPAR antagonist maybe measured by methods known in the art, such as those described andcited in Castelino et al., 2010 Arthritis Rheum. 2011 May; 63(5):1405-1415 or Swaney et al., J Pharmacol Exp Ther. 2011 March;336(3):693-700.

As used herein, an “ACC inhibitor” refers to any agent that is capableof binding and inhibiting Acetyl-CoA carboxylase (ACC). ACC inhibitorscan act as inhibitors or partial inhibitors of ACC. The agent can be achemical compound or biological molecule (e.g., a protein or antibody).The activity of an ACC inhibitor can be measured by methods known in theart, such as those described and cited in U.S. Pat. No. 8,969,557 and/orin U.S. Pat. No.10,208,063, both of which are incorporated herein byreference in their entirety.

As referred to herein, an “ASK1 inhibitor” can be any agent that iscapable of inactivating an apoptosis signal regulating kinase 1 (ASK1)protein. The agent can be a chemical compound or biological molecule(e.g., a protein or antibody). The ASK1 protein activity can be measuredby several different methods. For example, the activity of an ASK1protein can be determined based on the ability of the ASK1 protein tophosphorylate a substrate protein. Methods for identifying an ASK1inbibitor are known (see, e.g., U.S. 2007/0276050). Exemplary ASK1substrate proteins include MAPKK3, MAPKK4, MAPKK6, MAPKK7, or fragmentsthereof. The ASK1 protein activity can also be measured by thephosphorylation level of the ASK1 protein, for example, thephosphorylation level of a threonine residue in the ASK1 proteincorresponding to threonine 838 (T838) of a human full-length ASK1protein or threonine 845 (T845) of a mouse full-length ASK1 protein. Forexample, where the ASK1 protein comprises a full-length human ASK1protein sequence, an ASK1 inhibitor may attenuate phosphorylation ofT838 in the full-length human ASK1 protein sequence. A site-specificantibody against human ASK1 T838 or mouse ASK1 T845 may be used todetect the phosphohorylation level.

As used herein, a “FXR agonist” refers to any agent that is capable ofbinding and activating farnesoid X receptor (FXR) which can be referredto as bile acid receptor (BAR) or NR1H4 (nuclear receptor subfamily 1,group H, member 4) receptor. FXR agonists can act as agonists or partialagonists of FXR. The agent can be a chemical compound or biologicalmolecule (e.g., a protein or antibody). The activity of an FXR agonistcan be measured by several different methods, e.g., in an in vitro assayusing the fluorescence resonance energy transfer (FRET) cell free assayas described in Pellicciari, et al. Journal of Medicinal Chemistry, 2002vol. 15, No. 45:3569-72.

Compounds

In one embodiment, provided herein is a compound of Formula (I),

or a pharmaceutically acceptable salt thereof,

-   wherein:-   R¹ is hydrogen, C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₃₋₁₀    cycloalkyl, 3 to 10 membered heterocyclyl having 1 to 4 heteroatoms    independently selected from nitrogen, oxygen, and sulfur, 6 to 10    membered aryl, or 5 to 10 membered heteroaryl having 1 to 4    heteroatoms independently selected from nitrogen, oxygen, and    sulfur, wherein each alkyl, alkenyl, alkynyl, cycloalkyl,    heterocyclyl, aryl, or heteroaryl is optionally substituted with 1    to 4 R^(1A), which can be the same or different, wherein each R^(1A)    is independently selected from halogen, cyano, nitro, oxo, C₁₋₄    alkyl, C₃₋₁₀ cycloalkyl, 3 to 10 membered heterocyclyl having 1 to 4    heteroatoms independently selected from nitrogen, oxygen, and    sulfur, 6 to 10 membered aryl, 5 to 10 membered heteroaryl having 1    to 4 heteroatoms independently selected from nitrogen, oxygen, or    sulfur, —N(R^(1B1))(R^(1B2)), —O—R^(1B1), —S—R^(1B1),    —C(O)N(R^(1B1))(R^(1B2)), —NR^(1B1)C(O)R^(1B2),    —NR^(1B1)C(O)N(R^(1B2))(R^(1B3)), —S(O)₀₋₂R^(1B1),    —S(O)₂N(R^(1B1))(R^(1B2)), and —NR^(1B1)S(O)₂R^(1B2), wherein each    R^(1B1), R^(1B2), and R^(1B3) is independently hydrogen, C₁₋₆ alkyl,    or C₃₋₆ cycloalkyl,    -   wherein each R^(1A) alkyl, cycloalkyl, heterocyclyl, aryl, and        heteroaryl is optionally substituted with 1 to 4 R^(1C), which        can be the same or different, and wherein each R^(1C) is        independently C₁₋₄ alkyl, halogen, cyano, —O—R^(1D1), or        —N(R^(1D1))(R^(1D2)), wherein each R^(1D1) and R^(1D2) is        independently hydrogen or C₁₋₆ alkyl, and    -   wherein each R^(1B1), R^(1B2), and R^(1B3) alkyl and each        R^(1B1), R^(1B2), and R^(1B3) cycloalkyl is optionally        substituted with 1 to 3 halogens or-   R¹ is —O—R^(1D1) or —N(R^(1D1))(R^(1D2)), wherein each R^(1D1) and    R^(1D2) is independently hydrogen, C₁₋₆ alkyl, or C₃₋₆ cycloalkyl,    wherein each C₁₋₆ alkyl, or C₃₋₆ cycloalkyl is optionally    substituted with 1 to 4 R^(1E), which can be the same or different,    wherein each R^(1E) is independently selected from halogen, cyano,    hydroxy, oxo, C₁₋₄ alkyl, C₃₋₁₀ cycloalkyl, 3 to 10 membered    heterocyclyl having 1 to 4 heteroatoms independently selected from    nitrogen, oxygen, and sulfur, 6 to 10 membered aryl, 5 to 10    membered heteroaryl having 1 to 4 heteroatoms independently selected    from nitrogen, oxygen, or sulfur, —O—R^(1F1), —N(R^(1F1))(R^(1F2)),    —C(O)N(R^(1F1))(R^(1F2)), —NR^(1F1)C(O)R^(1F2), —S(O)₀₋₂R^(1F1),    —S(O)₂N(R^(1F1))(R^(1F2)), and —NR^(1F1)S(O)₂R^(1F2), wherein each    R^(1F1) and R^(1F2) is independently hydrogen or C₁₋₆ alkyl, wherein    each R^(1E) alkyl, cycloalkyl, aryl, and heteroaryl is optionally    substituted with 1 to 3 R^(1G), which can be the same or different,    and wherein each R^(1G) is independently C₁₋₄ alkyl, C₁₋₄ alkoxy,    hydroxy, halogen, or cyano;-   R² is hydrogen or C₁₋₆ alkyl optionally substituted with 1 to 3    substituents, which can be the same or different, independently    selected from halogen, cyano, C₁₋₄ alkoxy, and C₃₋₁₀ cycloalkyl; or-   R² is C₃₋₆ cycloalkyl optionally substituted with 1 to 3    substituents, which can be the same or different, independently    selected from halogen, cyano, C₁₋₄ alkoxy, and C₁₋₆ alkyl;-   each R³ is independently selected from deuterium, halogen, C₁₋₆    alkyl, C₃₋₆ cycloalkyl, —O—R^(2A1), and —N(R^(2A1))(R^(2A2)),    wherein the C₁₋₆ alkyl is optionally substituted with 1 to 3    substituents, which can be the same or different, independently    selected from C₁₋₄ alkoxy and halogen, and wherein each R^(2A1) and    R^(2A2) is independently hydrogen or C₁₋₃ alkyl optionally    substituted with 1 to 3 halogens, which can be the same or    different;-   n is 0, 1, 2, 3, or 4;-   R⁴ is C₁₋₆ alkyl optionally substituted with 1 to 3 substituents,    which can be the same or different, independently selected from    halogen, cyano, C₁₋₄ alkoxy, —C(O)N(R^(4A1)), and    —N(R^(4A1))(R^(4A2)), wherein each R^(4A1) and R^(4A2) is    independently hydrogen, C₁₋₆ alkyl, or C₃₋₁₀ cycloalkyl; or-   R⁴ is C₃₋₆ cycloalkyl or 3 to 6 membered heterocyclyl having 1 or 2    heteroatoms independently selected from nitrogen, oxygen, and    sulfur, wherein the cycloalkyl or heterocyclyl are optionally    substituted with 1 to 3 substituents, which can be the same or    different, independently selected from halogen, cyano, C₁₋₄ alkyl    and C₁₋₄ alkoxy;-   each of X¹, X², X³, and X⁴ is independently selected from CH and N;-   each Y¹ and Y² is independently hydrogen, deuterium, or C₁₋₆ alkyl    optionally substituted with 1 to 3 substituents, which can be the    same or different, independently selected from deuterium, halogen,    cyano, C₂₋₃ alkynyl, C₁₋₄ alkoxy, and —C(O)NH—(C₁₋₄H₃₋₉); and-   Z is C₁₋₈ alkyl, C₁₋₆ alkoxy, C₃₋₆ cycloalkyl, C₆₋₁₂ aryl, 3 to 12    membered heterocyclyl having 1 to 4 heteroatoms independently    selected from nitrogen, oxygen, and sulfur, or 5 to 12 membered    heteroaryl having 1 to 4 heteroatoms independently selected from    nitrogen, oxygen, and sulfur, wherein the alkyl, alkoxy, cycloalkyl,    aryl, heterocyclyl, or heteroaryl are each optionally substituted    with 1 to 3 substituents, which can be the same or different,    independently selected from halogen, cyano, C₁₋₄ alkyl, C₁₋₄ alkoxy,    and C₃₋₆ cycloalkyl, wherein the C₁₋₄ alkyl is optionally    substituted with 1 to 3 substituents, which can be the same or    different, selected from C₁₋₄ alkoxy and halogen; or-   Y¹ and Z together with the carbon to which they are attached form    C₃₋₆ cycloalkyl, C₆₋₁₂ aryl, 3 to 12 membered heterocyclyl having 1    to 4 heteroatoms independently selected from nitrogen, oxygen, and    sulfur, or 5 to 12 membered heteroaryl having 1 to 4 heteroatoms    independently selected from nitrogen, oxygen, and sulfur, wherein    the cycloalkyl, aryl, heterocyclyl, or heteroaryl are each    optionally substituted with 1 to 3 substituents, which can be the    same or different, independently selected from cyano, C₁₋₄ alkyl,    C₁₋₄ alkoxy, C₆₋₁₀ aryl, and halogen, wherein the C₁₋₄ alkyl is    optionally substituted with 1 to 3 substituents, which can be the    same or different, independently selected from C₁₋₄ alkoxy and    halogen, and wherein the C₆₋₁₀ aryl is optionally substituted with 1    to 3 substituents, which can be the same or different, independently    selected from C₁₋₄ alkyl, C₁₋₄ alkoxy, and halogen, and Y² is    hydrogen or deuterium.

In some embodiments of the compound of Formula I or pharmaceuticallyacceptable salt thereof

-   R¹ is hydrogen, C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₃₋₁₀    cycloalkyl, 3 to 10 membered heterocyclyl having 1 to 4 heteroatoms    independently selected from nitrogen, oxygen, and sulfur, 6 to 10    membered aryl, or 5 to 10 membered heteroaryl having 1 to 4    heteroatoms independently selected from nitrogen, oxygen, and    sulfur, wherein each alkyl, alkenyl, alkynyl, cycloalkyl,    heterocyclyl, aryl, or heteroaryl is optionally substituted with 1    to 4 R^(1A), which can be the same or different, wherein each R^(1A)    is independently selected from halogen, cyano, oxo, C₁₋₄ alkyl,    C₃₋₁₀ cycloalkyl, 3 to 10 membered heterocyclyl having 1 to 4    heteroatoms independently selected from nitrogen, oxygen, and    sulfur, 6 to 10 membered aryl, 5 to 10 membered heteroaryl having 1    to 4 heteroatoms independently selected from nitrogen, oxygen, or    sulfur, —N(R^(1B1))(R^(1B2)), —O—R^(1B1), —S—R^(1B1),    —C(O)N(R^(1B1))(R^(1B2)), —NR^(1B1)C(O)R^(1B2),    —NR^(1B1)C(O)N(R^(1B2))(R^(1B3)), —S(O)₀₋₂R^(1B1),    —S(O)₂N(R^(1B1))(R^(1B2)), and —NR^(1B1)S(O)₂R^(1B2), wherein each    R^(1B1), R^(1B2), and R^(1B3) is independently hydrogen, or C₁₋₆    alkyl,    -   wherein each R^(1A) alkyl, cycloalkyl, heterocyclyl, aryl, and        heteroaryl is optionally substituted with 1 to 4 R^(1C), which        can be the same or different, and wherein each R^(1C) is        independently C₁₋₄ alkyl, halogen, cyano, —O—R^(1D1), or        —N(R^(1D1))(R^(1D2)), and wherein each R^(1D1) and R^(1D2) is        independently hydrogen or C₁₋₆ alkyl; or-   R¹ is —O—R^(1D1) or —N(R^(1D1))(R^(1D2)), wherein each R^(1D1) and    R^(1D2) is independently hydrogen, C₁₋₆ alkyl, or C₃₋₆ cycloalkyl,    wherein each C₁₋₆ alkyl, or C₃₋₆ cycloalkyl is optionally    substituted with 1 to 4 R^(1E), which can be the same or different,    wherein each R^(1E) is independently selected from halogen, cyano,    hydroxy, oxo, C₁₋₄ alkyl, C₃₋₁₀ cycloalkyl, 3 to 10 membered    heterocyclyl having 1 to 4 heteroatoms independently selected from    nitrogen, oxygen, and sulfur, 6 to 10 membered aryl, 5 to 10    membered heteroaryl having 1 to 4 heteroatoms independently selected    from nitrogen, oxygen, or sulfur, —O—R^(1F1), —N(R^(1F1))(R^(1F2)),    —C(O)N(R^(1F1))(R^(1F2)), —NR^(1F1)C(O)R^(1F2), —S(O)₀₋₂R^(1F1),    —S(O)₂N(R^(1F1))(R^(1F2)), and —NR^(1F1)S(O)₂R^(1F2), wherein each    R^(1F1) and R^(1F2) is independently hydrogen or C₁₋₆ alkyl, wherein    each R^(1E) alkyl, cycloalkyl, aryl, and heteroaryl is optionally    substituted with 1 to 3 R^(1G), which can be the same or different,    and wherein each R^(1G) is independently C₁₋₄ alkyl, C₁₋₄ alkoxy,    hydroxy, halogen, or cyano;-   R² is hydrogen or C₁₋₆ alkyl optionally substituted with 1 to 3    substituents, which can be the same or different, independently    selected from halogen, cyano, C₁₋₄ alkoxy, and C₃₋₁₀ cycloalkyl; or-   R² is C₃₋₆ cycloalkyl optionally substituted with 1 to 3    substituents, which can be the same or different, independently    selected from halogen, cyano, C₁₋₄ alkoxy, and C₁₋₆ alkyl;-   each R³ is independently selected from deuterium, halogen, C₁₋₆    alkyl, C₃₋₆ cycloalkyl, —O—R^(2A1), and —N(R^(2A1))(R^(2A2)),    wherein the C₁₋₆ alkyl is optionally substituted with 1 to 3    substituents, which can be the same or different, independently    selected from C₁₋₄ alkoxy and halogen, and wherein each R^(2A1) and    R^(2A2) is independently hydrogen or C₁₋₃ alkyl optionally    substituted with 1 to 3 halogens, which can be the same or    different;-   n is 0, 1, 2, 3, or 4;-   R⁴ is C₁₋₆ alkyl optionally substituted with 1 to 3 substituents,    which can be the same or different, independently selected from    halogen, cyano, C₁₋₄ alkoxy, —C(O)N(R^(4A1)), and    —N(R^(4A1))(R^(4A2)), wherein each R^(4A1) and R^(4A2) is    independently hydrogen, C₁₋₆ alkyl, or C₃₋₁₀ cycloalkyl; or-   R⁴ is C₃₋₆ cycloalkyl or 3 to 6 membered heterocyclyl having 1 or 2    heteroatoms independently selected from nitrogen, oxygen, and    sulfur, wherein the cycloalkyl or heterocyclyl are optionally    substituted with 1 to 3 substituents, which can be the same or    different, independently selected from halogen, cyano, C₁₋₄ alkyl    and C₁₋₄ alkoxy;-   each of X¹, X², X³ and X⁴ is independently selected from CH and N;-   each Y¹ and Y² is independently hydrogen, deuterium, or C₁₋₆ alkyl    optionally substituted with 1 to 3 substituents, which can be the    same or different, independently selected from deuterium, halogen,    cyano, C₂₋₃ alkynyl, C₁₋₄ alkoxy, and —C(O)NH—(C₁₋₄H₃₋₉); and-   Z is C₁₋₈ alkyl, C₁₋₆ alkoxy, C₃₋₆ cycloalkyl, C₆₋₁₂ aryl, 3 to 12    membered heterocyclyl having 1 to 4 heteroatoms independently    selected from nitrogen, oxygen, and sulfur, or 5 to 12 membered    heteroaryl having 1 to 4 heteroatoms independently selected from    nitrogen, oxygen, and sulfur, wherein the alkyl, alkoxy, cycloalkyl,    aryl, heterocyclyl, or heteroaryl are each optionally substituted    with 1 to 3 substituents, which can be the same or different,    independently selected from halogen, cyano, C₁₋₄ alkyl, C₁₋₄ alkoxy,    and C₃₋₆ cycloalkyl, wherein the C₁₋₄ alkyl is optionally    substituted with 1 to 3 substituents, which can be the same or    different, selected from C₁₋₄ alkoxy and halogen; or-   Y¹ and Z together with the carbon to which they are attached form    C₃₋₆ cycloalkyl, C₆₋₁₂ aryl, 3 to 12 membered heterocyclyl having 1    to 4 heteroatoms independently selected from nitrogen, oxygen, and    sulfur, or 5 to 12 membered heteroaryl having 1 to 4 heteroatoms    independently selected from nitrogen, oxygen, and sulfur, wherein    the cycloalkyl, aryl, heterocyclyl, or heteroaryl are each    optionally substituted with 1 to 3 substituents, which can be the    same or different, independently selected from cyano, C₁₋₄ alkyl,    C₁₋₄ alkoxy, C₆₋₁₀ aryl, and halogen, wherein the C₁₋₄ alkyl is    optionally substituted with 1 to 3 substituents, which can be the    same or different, independently selected from C₁₋₄ alkoxy and    halogen, and wherein the C₆₋₁₀ aryl is optionally substituted with 1    to 3 substituents, which can be the same or different, independently    selected from C₁₋₄ alkyl, C₁₋₄ alkoxy, and halogen, and Y² is    hydrogen or deuterium.

In some embodiments, the compound of Formula (I), or pharmaceuticallyacceptable salt thereof, is a compound of Formula (Ia):

or pharmaceutically acceptable salt thereof.

In some embodiments of the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, R² is hydrogen.

In some embodiments of the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, R⁴ is C₁₋₃ alkyl optionallysubstituted with 1 to 3 substituents, which can be the same ordifferent, independently selected from cyano and F. In some embodimentsof the compound of Formula (I) or (Ia), or pharmaceutically acceptablesalt thereof, R⁴ is —CH₃.

In some embodiments of the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, X¹ is CH, X² is CH, X³ is CH,and X⁴ is CH.

In some embodiments of the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, X¹ is C(R³), X² is CH, X³ isCH, and X⁴ is CH.

In some embodiments of the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, X¹ is C(R³), X² is CH, X³ isC(R³), and X⁴ is CH.

In some embodiments of the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, X¹ is N, X² is CH, X³ is CH,and X⁴ is C(R³).

In some embodiments of the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, X¹ is CH, X² is N, X³ is CH,and X⁴ is C(R³).

In some embodiments of the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, X¹ is C(R³), X² is N, X³ isCH, and X⁴ is CH.

In some embodiments of the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, X¹ is C(R³), X² is N, X³ isCH, and X⁴ is C(R³).

In some embodiments of the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, X¹ is C(R³), X² is CH, X³ isC(R³), and X⁴ is CH.

In some embodiments of the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, X¹ is N, X² is CH, X³ is N,and X⁴ is C(R³).

In some embodiments of the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, X¹ is C(R³), X² is N, X³ is N,and X⁴ is CH.

In some embodiments of the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, X¹ is CH, X² is N, X³ is N,and X⁴ is CH.

In some embodiments of the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, X¹ is N, X² is CH, X³ is CH,and X⁴ is CH.

In some embodiments of the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, X¹ is N, X² is CH, X³ is N,and X⁴ is CH.

In some embodiments of the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, X¹ is CH, X² is N, X³ isC(R³), and X⁴ is CH.

In some embodiments of the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, X¹ is CH, X² is N, X³ is CH,and X⁴ is CH.

In some embodiments of the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, Y² is hydrogen.

In some embodiments, the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, is a compound of Formula(IIa):

or a pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, is a compound of Formula(IIb):

or a pharmaceutically acceptable salt thereof, wherein each R³ can bethe same or different.

In some embodiments, the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, is a compound of Formula(IIc):

or a pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, is a compound of Formula(IId):

or a pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, is a compound of Formula(IIe):

or a pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, is a compound of Formula(IIf):

or a pharmaceutically acceptable salt thereof, wherein each R³ can bethe same or different.

In some embodiments, the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, is a compound of Formula(IIg):

or a pharmaceutically acceptable salt thereof, wherein each R³ can bethe same or different.

In some embodiments, the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, is a compound of Formula(IIh):

or a pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, is a compound of Formula(IIi):

or a pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, is a compound of Formula(IIj):

or a pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, is a compound of Formula(IIk):

or a pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, is a compound of Formula(IIl):

or a pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, is a compound of Formula(IIm):

or a pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, is a compound of Formula(IIn):

or a pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, is a compound of Formula(IIo):

or a pharmaceutically acceptable salt thereof.

In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹is hydrogen.

In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹is R¹ is C₁₋₆ alkyl, C₂₋₆ alkenyl, or C₂₋₆ alkynyl, each optionallysubstituted with 1 to 4 R^(1A), which can be the same or different,wherein each R^(1A) is independently selected from halogen, cyano,nitro, oxo, C₁₋₄ alkyl, C₃₋₁₀ cycloalkyl, 3 to 10 membered heterocyclylhaving 1 to 4 heteroatoms independently selected from nitrogen, oxygen,and sulfur, 6 to 10 membered aryl, 5 to 10 membered heteroaryl having 1to 4 heteroatoms independently selected from nitrogen, oxygen or sulfur—N(R^(1B1))(R^(1B2)), —O—R^(1B1), —S—R^(1B1), —C(O)N(R^(1B1))(R^(1B2)),—NR^(1B1)C(O)R^(1B2), —NR^(1B1)C(O)N(R^(1B2))(R^(1B3)), —S(O)₀₋₂R^(1B1),—S(O)₂N(R^(1B1))(R^(1B2)), and —NR^(1B1)S(O)₂R^(1B2), wherein eachR^(1B1), R^(1B2), and R^(1B3) is independently hydrogen, C₁₋₆ alkyl, orC₃₋₆ cycloalkyl, wherein each R^(1A) alkyl, cycloalkyl, heterocyclyl,aryl, and heteroaryl is optionally substituted with 1 to 4 R^(1C), whichcan be the same or different, wherein each R^(1C) is independently C₁₋₄alkyl, halogen, cyano, —O—R^(1D1), or —N(R^(1D1))(R^(1D2)), wherein eachR^(1D1) and R^(1D2) is independently hydrogen or C₁₋₆ alkyl, and whereineach R^(1B1), R^(1B2), and R^(1B3) alkyl and each R^(1B1), R^(1B2), andR^(1B3) cycloalkyl is optionally substituted with 1 to 3 halogens. Insome embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹is R¹ is C₁₋₆ alkyl, C₂₋₆ alkenyl, or C₂₋₆ alkynyl, each optionallysubstituted with 1 to 4 R^(1A), which can be the same or different,wherein each R^(1A) is independently selected from halogen, cyano, oxo,C₁₋₄ alkyl, C₃₋₁₀ cycloalkyl, 3 to 10 membered heterocyclyl having 1 to4 heteroatoms independently selected from nitrogen, oxygen, and sulfur,6 to 10 membered aryl, 5 to 10 membered heteroaryl having 1 to 4heteroatoms independently selected from nitrogen, oxygen, or sulfur,—N(R^(1B1))(R^(1B2)), —O—R^(1B1), —S—R^(1B1), —C(O)N(R^(1B1))(R^(1B2)),—NR^(1B1)C(O)R^(1B2), —NR^(1B1)C(O)N(R^(1B2))(R^(1B3)), —S(O)₀₋₂R^(1B1),—S(O)₂N(R^(1B1))(R^(1B2)), and —NR^(1B1)S(O)₂R^(1B2), wherein eachR^(1B1), R^(1B2), and R^(1B3) is independently hydrogen or C₁₋₆ alkyl,wherein each R^(1A) alkyl, cycloalkyl, heterocyclyl, aryl, andheteroaryl is optionally substituted with 1 to 4 R^(1C), which can bethe same or different, wherein each R^(1C) is independently C₁₋₄ alkyl,halogen, cyano, —O—R^(1D1), or —N(R^(1D1))(R^(1D2)), and wherein eachR^(1D1) and R^(1D2) is independently hydrogen or C₁₋₆ alkyl. In someembodiments of the compound of Formula (I), (Ia), (IIa), (IIb), (IIc),(IId), (IIe), (IIf), (IIg), (IIh), or (IIi), or pharmaceuticallyacceptable salt thereof, R¹ is C₁₋₆ alkyl or C₂₋₆ alkynyl, eachoptionally substituted with 1 to 4 R^(1A), which can be the same ordifferent, wherein each R^(1A) is independently selected from halogen,cyano, hydroxy, C₁₋₄ alkoxy, and C₃₋₆ cycloalkyl. In some embodiments,each halogen in R^(1A) or R^(1C) is —F. In some embodiments, each R^(1A)is independently selected from —F, —CN, —OH, —OCH₃, or cyclopropyl. Insome embodiments, each halogen in R^(1A) or R^(1C) is —F. In someembodiments of the compound of Formula (I), (Ia), (IIa), (IIb), (IIc),(IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm),(IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹ is C₁₋₆alkyl or C₂₋₆ alkynyl, each optionally substituted with 1 to 4 R^(1A),which can be the same or different, wherein each R^(1A) is independentlyselected from —F, —CN, —OH, —OCH₃, or cyclopropyl. In some embodimentsof the compound of Formula (I), (Ia), (IIa), (IIb), (IIc), (IId), (IIe),(IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm), (IIn), or (IIo),or pharmaceutically acceptable salt thereof, R¹ is —CH₃, —CHF₂, —CF₃,

In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹is —O—R^(1D1) or —N(R^(1D1))(R^(1D2)), wherein each R^(1D1) and R^(1D2)is independently hydrogen, C₁₋₆ alkyl, or C₃₋₆ cycloalkyl, wherein eachC₁₋₆ alkyl, or C₃₋₆ cycloalkyl is optionally substituted with 1 to 4R^(1E), which can be the same or different, wherein each R^(1E) isindependently selected from halogen, cyano, hydroxy, oxo, C₁₋₄ alkyl,C₃₋₁₀ cycloalkyl, 3 to 10 membered heterocyclyl having 1 to 4heteroatoms independently selected from nitrogen, oxygen, and sulfur, 6to 10 membered aryl, 5 to 10 membered heteroaryl having 1 to 4heteroatoms independently selected from nitrogen, oxygen, or sulfur,—O—R^(1F1), —N(R^(1F1))(R^(1F2)), —C(O)N(R^(1F1))(R^(1F2)),—NR^(1F1)C(O)R^(1F2), —S(O)₀₋₂R^(1F1), —S(O)₂N(R^(1F1))(R^(1F2)), and—NR^(1F1)S(O)₂R^(1F2), wherein each R^(1F1) and R^(1F2) is independentlyhydrogen or C₁₋₆ alkyl, wherein each R^(1E) alkyl, cycloalkyl, aryl, andheteroaryl is optionally substituted with 1 to 3 R^(1G), which can bethe same or different, and wherein each R^(1G) is independently C₁₋₄alkyl, C₁₋₄ alkoxy, hydroxy, halogen, or cyano. In some embodiments ofthe compound of Formula (I), (Ia), (IIa), (IIb), (IIc), (IId), (IIe),(IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm), (IIn), or (IIo),or pharmaceutically acceptable salt thereof, R¹ is —O—R^(1D1) or—N(R^(1D1))(R^(1D2)), wherein each R^(1D1) and R^(1D2) is independentlyhydrogen, C₁₋₆ alkyl, or C₃₋₆ cycloalkyl, wherein each C₁₋₆ alkyl, orC₃₋₆ cycloalkyl is optionally substituted with 1 to 3 R^(1E), which canbe the same or different, wherein each R^(1E) is independently selectedfrom halogen and —C(O)N(R^(1F1))(R^(1F1)), wherein each —R^(1F1) and—R^(1F1) is independently hydrogen or C₁₋₄ alkyl. In some embodiments,each —R^(1E) halogen is —F. In some embodiments, each —R^(1G) halogen is—F. In some embodiments of the compound of Formula (I), (Ia), (IIa),(IIb), (IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk),(IIl), (IIm), (IIn), or (IIo), or pharmaceutically acceptable saltthereof, R¹ is —O—R^(1D1) or —N(R^(1D1))(R^(1D2)), wherein each R^(1D1)and R^(1D2) is independently —H, —CH₃, —C₂H₅, or —C(CH₃)₃. In someembodiments of the compound of Formula (I), (Ia), (IIa), (IIb), (IIc),(IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm),(IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹ is

In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹is C₃₋₁₀ cycloalkyl optionally substituted with 1 to 4 R^(1A), which canbe the same or different, wherein each R^(1A) is independently selectedfrom halogen, cyano, nitro, oxo, C₁₋₄ alkyl, C₃₋₁₀ cycloalkyl, 3 to 10membered heterocyclyl having 1 to 4 heteroatoms independently selectedfrom nitrogen, oxygen, and sulfur, 6 to 10 membered aryl, 5 to 10membered heteroaryl having 1 to 4 heteroatoms independently selectedfrom nitrogen, oxygen, or sulfur, —N(R^(1B1))(R^(1B2)), —O—R^(1B1),—S—R^(1B1), —C(O)N(R^(1B1))(R^(1B2)), —NR^(1B1)C(O)R^(1B2),—NR^(1B1)C(O)N(R^(1B2))(R^(1B3)), —S(O)₀₋₂R^(1B1),—S(O)₂N(R^(1B1))(R^(1B2)), and —NR^(1B1)S(O)₂R^(1B2), wherein eachR^(1B1), R^(1B2), and R^(1B3) is independently hydrogen, C₁₋₆ alkyl, or—C₃₋₆ cycloalkyl, wherein each R^(1A) alkyl, cycloalkyl, heterocyclyl,aryl, and heteroaryl is optionally substituted with 1 to 4 R^(1C), whichcan be the same or different, and wherein each R^(1C) is independentlyC₁₋₄ alkyl, halogen, cyano, —O—R^(1D1), or —N(R^(1D1))(R^(1D2)), whereineach R^(1D1) and R^(1D2) is independently hydrogen or C₁₋₆ alkyl, andwherein each R^(1B1) and R^(1B2) alkyl and each R^(1B1) and R^(1B2)cycloalkyl is optionally substituted with 1 to 3 halogens. In someembodiments of the compound of Formula (I), (Ia), (IIa), (IIb), (IIc),(IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm),(IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹ isC₃₋₁₀ cycloalkyl optionally substituted with 1 to 4 R^(1A), which can bethe same or different, wherein each R^(1A) is independently selectedfrom halogen, cyano, oxo, C₁₋₄ alkyl, C₃₋₁₀ cycloalkyl, 3 to 10 memberedheterocyclyl having 1 to 4 heteroatoms independently selected fromnitrogen, oxygen, and sulfur, 6 to 10 membered aryl, 5 to 10 memberedheteroaryl having 1 to 4 heteroatoms independently selected fromnitrogen, oxygen, or sulfur, —N(R^(1B1))(R^(1B2)), —O—R^(1B1),—S—R^(1B1), —C(O)N(R^(1B1))(R^(1B2)), —NR^(1B1)C(O)R^(1B2),—NR^(1B1)C(O)N(R^(1B2))(R^(1B3)), —S(O)₀₋₂R^(1B1),—S(O)₂N(R^(1B1))(R^(1B2)), and —NR^(1B1)S(O)₂R^(1B2), wherein eachR^(1B1), R^(1B2), and R^(1B3) is independently hydrogen or C₁₋₆ alkyl,wherein each R^(1A) alkyl, cycloalkyl, heterocyclyl, aryl, andheteroaryl is optionally substituted with 1 to 4 R^(1C), which can bethe same or different, and wherein each R^(1C) is independently C₁₋₄alkyl, halogen, cyano, —O—R^(1D1), or —N(R^(1D1))(R^(1D2)), and whereineach R^(1D1) and R^(1D2) is independently hydrogen or C₁₋₆ alkyl. Insome embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹is C₃₋₁₀ cycloalkyl optionally substituted with 1 to 4 R^(1A), which canbe the same or different, wherein each R^(1A) is independently selectedfrom halogen, cyano, nitro, oxo, C₁₋₄ alkyl, 3 to 6 memberedheterocyclyl having 1 to 2 heteroatoms independently selected fromnitrogen, oxygen, and sulfur, 5 or 6 membered heteroaryl having 1 or 2heteroatoms independently selected from nitrogen or oxygen, —OR^(1B1),and —C(O)N(R^(1B1))(R^(1B2)), wherein each R^(1B1) and R^(1B2) isindependently hydrogen, C₁₋₄ alkyl, or C₃₋₆ cycloalkyl, and wherein eachR^(1A) C₁₋₄ alkyl is optionally substituted with 1 to 3 halogens, andeach heteroaryl in R^(1A) is optionally substituted with 1 to 3 C₁₋₄alkyl, and wherein each R^(1B1) and R^(1B2) alkyl and each R^(1B1) andR^(1B2) cycloalkyl is optionally substituted with 1 to 3 halogens. Insome embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹is C₃₋₁₀ cycloalkyl optionally substituted with 1 to 4 R^(1A), which canbe the same or different, wherein each R^(1A) is independently selectedfrom halogen, cyano, oxo, C₁₋₄ alkyl, 3 to 6 membered heterocyclylhaving 1 to 2 heteroatoms independently selected from nitrogen, oxygen,and sulfur, 5 or 6 membered heteroaryl having 1 or 2 heteroatomsindependently selected from nitrogen or oxygen, —OR^(1B1), and—C(O)N(R^(1B1))(R^(1B2)), wherein each R^(1B1) and R^(1B2) isindependently hydrogen or C₁₋₄ alkyl, and wherein each R^(1A) C₁₋₄ alkylis optionally substituted with 1 to 3 halogens, and each heteroaryl inR^(1A) is optionally substituted with 1 to 3 C₁₋₄ alkyl. In someembodiments of the compound of Formula (I), (Ia), (IIa), (IIb), (IIc),(IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm),(IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹ iscyclopropyl or cyclobutyl, each optionally substituted with 1 to 4R^(1A), which can be the same or different, each independently selectedfrom —F, —Cl, —CN, ═O, —OH, —CH₃, —CH₂F, —CHF₂, —CF₃, —CH₂—OH, —CH₂—NH₂,—OCH₃, —NH₂, —NH—CH₂—CF₃,

—NO₂, cyclopropyl, isoxazyl, phenyl, pyridyl, and —C(O)NH₂, wherein eachisoxazyl or pyridyl is optionally substituted with 1 to 2 —F or —CH₃. Insome embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹is cyclopropyl or cyclobutyl, each optionally substituted with 1 to 4R^(1A), which can be the same or different, each independently selectedfrom —F, —Cl, —CN, ═O, —OH, —CH₃, —CH₂F, —CHF₂, —CF₃, —CH₂—OH, —CH₂—NH₂,—OCH₃, —NH₂, cyclopropyl, isoxazyl, phenyl, pyridyl, and —C(O)NH₂,wherein each isoxazyl or pyridyl is optionally substituted with 1 to 2—F or —CH₃. In some embodiments of the compound of Formula (I), (Ia),(IIa), (IIb), (IIc), (IId), (IIe), (IIf), (IIg), (IIh), or (IIi), orpharmaceutically acceptable salt thereof, R¹ is cyclopropyl orcyclobutyl, each optionally substituted with 1 to 4 R^(1A), which can bethe same or different, each independently selected from —F, —Cl, —CN,═O, —OH, —CH₃, —CH₂F, —CHF₂, —CF₃, —OCH₃, isoxazyl, pyridyl, and—C(O)NH₂, wherein each isoxazyl or pyridyl is optionally substitutedwith 1 to 2 —CH₃. In some embodiments of the compound of Formula (I),(Ia), (IIa), (IIb), (IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi),(IIj), (IIk), (IIl), (IIm), (IIn), or (IIo), or pharmaceuticallyacceptable salt thereof, R¹ is

In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹is

In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹is

In some embodiments, the C₃₋₁₀ cycloalkyl is a C₅₋₁₀ bicycliccycloalkyl. In some embodiments the C₅₋₁₀ bicyclic cycloalkyl is a C₅₋₈bridged bicyclic cycloalkyl. In some embodiments, the C₅₋₈ bridgedbicyclic cycloalkyl is bicyclopentanyl or bicyclooctanyl, eachoptionally substituted with 1 to 3 substituents, which can be the sameor different, each independently selected from —F, —Cl, —OH, —CN, —CH₃,—CH₂F, —CHF₂, —CF₃, —O—CH₃, —NH—CO—CH₃, —SO₂—CH₃, and oxetanyl. In someembodiments, the C₅₋₈ bridged bicyclic cycloalkyl is bicyclopentanyl orbicyclooctanyl, each optionally substituted with 1 to 3 substituents,which can be the same or different, each independently selected from —F,—Cl, —OH, —CN, —CH₃, —CH₂F, —CHF₂, —CF₃, —O—CH₃, and oxetanyl. In someembodiments of the compound of Formula (I), (Ia), (IIa), (IIb), (IIc),(IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm),(IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹ is

In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), or (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), (IIo), or pharmaceutically acceptable salt thereof, R¹ is

In some embodiments the C₅₋₁₀ bicyclic cycloalkyl is a C₅₋₁₀ spirobicyclic cycloalkyl. In some embodiments, the C₅₋₁₀ spiro bicycliccycloalkyl is spiropentanyl, spirohexanyl, spiroheptanyl, orspirodecanyl, each optionally substituted with 1 to 4 R^(1A), which canbe the same or different, wherein each R^(1A) is each independentlyselected from —F, —Cl, —OH, —CH₃, —CH₂F, —CHF₂, —CF₃, —CN, and —O—CH₃.In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹is

In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹is

In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIa),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹is 3 to 10 membered heterocyclyl having 1 to 4 heteroatoms independentlyselected from nitrogen, oxygen, and sulfur, optionally substituted with1 to 4 R^(1A), which can be the same or different, wherein each R^(1A)is independently selected from halogen, cyano, nitro, oxo, C₁₋₄ alkyl,C₃₋₁₀ cycloalkyl, 3 to 10 membered heterocyclyl having 1 to 4heteroatoms independently selected from nitrogen, oxygen, and sulfur, 6to 10 membered aryl, 5 to 10 membered heteroaryl having 1 to 4heteroatoms independently selected from nitrogen, oxygen, or sulfur,—N(R^(1B1))(R^(1B2)), —O—R^(1B1), —S—R^(1B1), —C(O)N(R^(1B1))(R^(1B2)),—NR^(1B1)C(O)R^(1B2), —NR^(1B1)C(O)N(R^(1B2))(R^(1B3)), —S(O)₀₋₂R^(1B1),—S(O)₂N(R^(1B1))(R^(1B2)), and —NR^(1B1)S(O)₂R^(1B2), wherein eachR^(1B1), R^(1B2), and R^(1B3) is independently hydrogen, C₁₋₆ alkyl, orC₃₋₆ cycloalkyl, wherein each R^(1A) alkyl, cycloalkyl, heterocyclyl,aryl, and heteroaryl is optionally substituted with 1 to 4 R^(1C), whichcan be the same or different, and wherein each R^(1C) is independentlyC₁₋₄ alkyl, halogen, cyano, —O—R^(1D1), or —N(R^(1D1))(R^(1D2)), whereineach R^(1D1) and R^(1D2) is independently hydrogen or C₁₋₆ alkyl, andwherein each R^(1B1) and R^(1B2) alkyl and each R^(1B1) and R^(1B2)cycloalkyl is optionally substituted with 1 to 3 halogens. In someembodiments of the compound of Formula (I), (Ia), (IIa), (IIb), (IIc),(IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm),(IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹ is 3 to10 membered heterocyclyl having 1 to 4 heteroatoms independentlyselected from nitrogen, oxygen, and sulfur, optionally substituted with1 to 4 R^(1A), which can be the same or different, wherein each R^(1A)is independently selected from halogen, cyano, oxo, C₁₋₄ alkyl, C₃₋₁₀cycloalkyl, 3 to 10 membered heterocyclyl having 1 to 4 heteroatomsindependently selected from nitrogen, oxygen, and sulfur, 6 to 10membered aryl, 5 to 10 membered heteroaryl having 1 to 4 heteroatomsindependently selected from nitrogen, oxygen or sulfur,—N(R^(1B1))(R^(1B2)), —O—R^(1B1), —S—R^(1B1), —C(O)N(R^(1B1))(R^(1B2)),—NR^(1B1)C(O)R^(1B2), —NR^(1B1)C(O)N(R^(1B2))(R^(1B3)), —S(O)₀₋₂R^(1B1),—S(O)₂N(R^(1B1))(R^(1B2)), and —NR^(1B1)S(O)₂R^(1B2), wherein eachR^(1B1), R^(1B2), and R^(1B3) is independently hydrogen or C₁₋₆ alkyl,wherein each R^(1A) alkyl, cycloalkyl, heterocyclyl, aryl, andheteroaryl is optionally substituted with 1 to 4 R^(1C), which can bethe same or different, and wherein each R^(1C) is independently C₁₋₄alkyl, halogen, cyano, —O—R^(1D1), or —N(R^(1D1))(R^(1D2)), wherein eachR^(1D1) and R^(1D2) is independently hydrogen or C₁₋₆ alkyl. In someembodiments of the compound of Formula (I), (Ia), (IIa), (IIb), (IIc),(IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm),(IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹ is 3 to8 membered heterocyclyl having 1 to 2 heteroatoms independently selectedfrom nitrogen, oxygen, and sulfur, optionally substituted with 1 to 4R^(1A), which can be the same or different, each independently selectedfrom halogen, cyano, oxo, or C₁₋₄ alkyl, wherein each R^(1A) C₁₋₄ alkylis optionally substituted with 1 to 3 R^(1C), which can be the same ordifferent, and wherein each R^(1C) is independently C₁₋₄ alkoxy,halogen, or cyano. In some embodiments of the compound of Formula (I),(Ia), (IIa), (IIb), (IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi),(IIj), (IIk), (IIl), (IIm), (IIn), or (IIo), or pharmaceuticallyacceptable salt thereof, R¹ is azetidinyl, oxetyl, thietanyl,pyrrolidinyl, dioxolanyl, tetrahydropyranyl, piperidinyl, ormorpholinyl, each optionally substituted with 1 to 4 R^(1A), which canbe the same or different, each independently selected from —F, —Cl, —OH,—CN, —CH₃, —CH₂F, —CHF₂, —CF₃, —C₂H₅, —CH₂—CF₃, and —O—CH₃. In someembodiments of the compound of Formula (I), (Ia), (IIa), (IIb), (IIc),(IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm),(IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹ isazetidinyl, oxetyl, thietanyl, pyrrolidinyl, dioxolanyl,tetrahydropyranyl, or morpholinyl, each optionally substituted with 1 to4 R^(1A), which can be the same or different, each independentlyselected from —F, —Cl, —OH, —CN, —CH₃, —CH₂F, —CHF₂, —CF₃, and —O—CH₃.In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹is

In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹is

In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, theR¹ 3 to 10 membered heterocyclyl forms a bicyclic heterocyclyl. In someembodiments, the bicyclic heterocyclyl is a bridged bicyclicheterocyclyl. In some embodiments, the bridged bicyclic heterocyclyl isan oxabicyclohexanyl optionally substituted with 1 to 4 R^(1A), whichcan be the same or different, wherein each R^(1A) is independentlyselected from —F, —Cl, —OH, —CN, —CH₃, —CH₂F, —CHF₂, —CF₃, and —O—CH₃.In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹is

In some embodiments the bicyclic heterocyclyl is a fused bicyclicheterocyclyl. In some embodiments the fused bicyclic heterocyclyl is anoxabicyclohexanyl optionally substituted with 1 to 4 R^(1A), which canbe the same or different, wherein each R^(1A) is independently selectedfrom —F, —Cl, —OH, —CN, —CH₃, —CH₂F, —CHF₂, —CF₃, and —O—CH₃. In someembodiments of the compound of Formula (I), (Ia), (IIa), (IIb), (IIc),(IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm),(IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹ is

In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (Ilk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹is

In some embodiments, the bicyclic heterocyclyl is a spiro bicyclicheterocyclyl. In some embodiments, the spiro bicyclic heterocyclyl is anoxaspiroheptane optionally substituted with 1 to 4 substituents, whichcan be the same or different, each independently selected from —F, —Cl,—OH, —CN, —CH₃, —CH₂F, —CHF₂, —CF₃, and —O—CH₃. In some embodiments ofthe compound of Formula (I), (Ia), (IIa), (IIb), (IIc), (IId), (IIe),(IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm), (IIn), or (IIo),or pharmaceutically acceptable salt thereof, R¹ is

In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (Ilk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹is 6 to 10 membered aryl optionally substituted with 1 to 4 R^(1A),which can be the same or different, wherein each R^(1A) is independentlyselected from halogen, cyano, nitro, oxo, C₁₋₄ alkyl, C₃₋₁₀ cycloalkyl,3 to 10 membered heterocyclyl having 1 to 4 heteroatoms independentlyselected from nitrogen, oxygen, and sulfur, 6 to 10 membered aryl, 5 to10 membered heteroaryl having 1 to 4 heteroatoms independently selectedfrom nitrogen, oxygen, or sulfur, —N(R^(1B1))(R^(1B2)), —O—R^(1B1),—S—R^(1B1), —C(O)N(R^(1B1))(R^(1B2)), —NR^(1B1)C(O)R^(1B2),—NR^(1B1)C(O)N(R^(1B2))(R^(1B3)), —S(O)₀₋₂R^(1B1),—S(O)₂N(R^(1B1))(R^(1B2)), and —NR^(1B1)S(O)₂R^(1B2), wherein eachR^(1B1), R^(1B2), and R^(1B3) is independently hydrogen, C₁₋₆ alkyl, orC₃₋₆ cycloalkyl, wherein each R^(1A) alkyl, cycloalkyl, heterocyclyl,aryl, and heteroaryl is optionally substituted with 1 to 4 R^(1C), whichcan be the same or different, and wherein each R^(1C) is independentlyC₁₋₄ alkyl, halogen, cyano, —O—R^(1D1), or —N(R^(1D1))(R^(1D2)), whereineach R^(1D1) and R^(1D2) is independently hydrogen or C₁₋₆ alkyl, andwherein each R^(1B1) and R^(1B2) alkyl and each R^(1B1) and R^(1B2)cycloalkyl is optionally substituted with 1 to 3 halogens. In someembodiments of the compound of Formula (I), (Ia), (IIa), (IIb), (IIc),(IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm),(IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹ is 6 to10 membered aryl optionally substituted with 1 to 4 R^(1A), which can bethe same or different, wherein each R^(1A) is independently selectedfrom halogen, cyano, oxo, C₁₋₄ alkyl, C₃₋₁₀ cycloalkyl, 3 to 10 memberedheterocyclyl having 1 to 4 heteroatoms independently selected fromnitrogen, oxygen, and sulfur, 6 to 10 membered aryl, 5 to 10 memberedheteroaryl having 1 to 4 heteroatoms independently selected fromnitrogen, oxygen, or sulfur, —N(R^(1B1))(R^(1B2)), —O—R^(1B1),—S—R^(1B1), —C(O)N(R^(1B1))(R^(1B2)), —NR^(1B1)C(O)R^(1B2),—NR^(1B1)C(O)N(R^(1B2))(R^(1B3)), —S(O)₀₋₂R^(1B1),—S(O)₂N(R^(1B1))(R^(1B2)), and —NR^(1B1)S(O)₂R^(1B2), wherein eachR^(1B1), R^(1B2), and R^(1B3) is independently hydrogen or C₁₋₆ alkyl,wherein each R^(1A) alkyl, cycloalkyl, heterocyclyl, aryl, andheteroaryl is optionally substituted with 1 to 4 R^(1C), which can bethe same or different, and wherein each R^(1C) is independently C₁₋₄alkyl, halogen, cyano, —O—R^(1D1), or —N(R^(1D1))(R^(1D2)), wherein eachR^(1D1) and R^(1D2) is independently hydrogen or C₁₋₆ alkyl. In someembodiments, R¹ is phenyl optionally substituted with 1 to 4 R^(1A),which can be the same or different, wherein each R^(1A) is independentlyselected from halogen, cyano, C₁₋₃ alkyl, or C₁₋₄ alkoxy. In someembodiments, R¹ is phenyl optionally substituted with 1 to 3 R^(1A),which can be the same or different, wherein each R^(1A) is independentlyselected from —F, —Cl, —CN, or —CH₃.

In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, R¹is 5 to 10 membered heteroaryl having 1 to 4 heteroatoms independentlyselected from nitrogen, oxygen, and sulfur, optionally substituted with1 to 4 R^(1A), which can be the same or different, wherein each R^(1A)is independently selected from halogen, cyano, nitro, oxo, C₁₋₄ alkyl,C₃₋₁₀ cycloalkyl, 3 to 10 membered heterocyclyl having 1 to 4heteroatoms independently selected from nitrogen, oxygen, and sulfur, 6to 10 membered aryl, 5 to 10 membered heteroaryl having 1 to 4heteroatoms independently selected from nitrogen, oxygen, or sulfur,—N(R^(1B1))(R^(1B2)), —O—R^(1B1), —S—R^(1B1), —C(O)N(R^(1B1))(R^(1B2)),—NR^(1B1)C(O)R^(1B2), —NR^(1B1)C(O)N(R^(1B2))(R^(1B3)), 13S(O)₀₋₂R^(1B1), —S(O)₂N(R^(1B1))(R^(1B2)), and —NR^(1B1)S(O)₂R^(1B2),wherein each R^(1B1), R^(1B2), and R^(1B3) is independently hydrogen,C₁₋₆ alkyl, or C₃₋₆ cycloalkyl, wherein each R^(1A) alkyl, cycloalkyl,heterocyclyl, aryl, and heteroaryl is optionally substituted with 1 to 4R^(1C), which can be the same or different, and wherein each R^(1C) isindependently C₁₋₄ alkyl, halogen, cyano, —O—R^(1D1), or—N(R^(1D1))(R^(1D2)), wherein each R^(1D1) and R^(1D2) is independentlyhydrogen or C₁₋₆ alkyl, and wherein each R^(1B1) and R^(1B2) alkyl andeach R^(1B1) and R^(1B2) cycloalkyl is optionally substituted with 1 to3 halogens. In some embodiments of the compound of Formula (I), (Ia),(IIa), (IIb), (IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj),(IIk), (IIl), (IIm), (IIn), or (IIo), or pharmaceutically acceptablesalt thereof, R¹ is 5 to 10 membered heteroaryl having 1 to 4heteroatoms independently selected from nitrogen, oxygen, and sulfur,optionally substituted with 1 to 4 R^(1A), which can be the same ordifferent, wherein each R^(1A) is independently selected from halogen,cyano, oxo, C₁₋₄ alkyl, C₃₋₁₀ cycloalkyl, 3 to 10 membered heterocyclylhaving 1 to 4 heteroatoms independently selected from nitrogen, oxygen,and sulfur, 6 to 10 membered aryl, 5 to 10 membered heteroaryl having 1to 4 heteroatoms independently selected from nitrogen, oxygen, orsulfur, —N(R^(1B1))(R^(1B2)), —O—R^(1B1), —S—R^(1B1),—C(O)N(R^(1B1))(R^(1B2)), —NR^(1B1)C(O)R^(1B2),—NR^(1B1)C(O)N(R^(1B2))(R^(1B3)), —S(O)₀₋₂R^(1B1),—S(O)₂N(R^(1B1))(R^(1B2)), and —NR^(1B1)S(O)₂R^(1B2), wherein eachR^(1B1), R^(1B2), and R^(1B3) is independently hydrogen or C₁₋₆ alkyl,wherein each R^(1A) alkyl, cycloalkyl, heterocyclyl, aryl, andheteroaryl is optionally substituted with 1 to 4 R^(1C), which can bethe same or different, and wherein each R^(1C) is independently C₁₋₄alkyl, halogen, cyano, —O—R^(1D1), or —N(R^(1D1))(R^(1D2)), wherein eachR^(1D1) and R^(1D2) is independently hydrogen or C₁₋₆ alkyl. In someembodiments, R¹ is imidazolyl, pyrazolyl, pyridinyl, oxazolyl,isoxazolyl, oxadiazolyl, pyridinonyl, pyrimidinyl, pyridazinyl,benzoisoxazolyl, pyrazolopyridinyl, imidazopyridinyl, orbenzoimidazolyl, each optionally substituted with 1 to 4 R^(1A), whichcan be the same or different, wherein each R^(1A) is independentlyselected from halogen, cyano, oxo, C₁₋₄ alkyl, C₃₋₁₀ cycloalkyl, 3 to 10membered heterocyclyl having 1 to 4 heteroatoms independently selectedfrom nitrogen and oxygen, —N(R^(1B1))(R^(1B2)), —O—R^(1B1), and—S(O)₀₋₂R^(1B1), wherein each R^(1B1) and R^(1B2) is independentlyhydrogen or C₁₋₆ alkyl, wherein each R^(1A) alkyl, cycloalkyl, andheterocyclyl, is optionally substituted with 1 to 4 R^(1C), which can bethe same or different, and wherein each R^(1C) is independently C₁₋₄alkyl, halogen, or cyano. In some embodiments, R¹ is imidazolyl,pyrazolyl, pyridinyl, oxazolyl, isoxazolyl, oxadiazolyl, pyridinonyl,pyrimidinyl, pyridazinyl, benzoisoxazolyl, pyrazolopyridinyl,imidazopyridinyl, or benzoimidazolyl, each optionally substituted with 1to 4 R^(1A), which can be the same or different, wherein each R^(1A) isindependently selected from halogen, cyano, oxo, methyl, cyclopropyl,morpholinyl, —N(R^(1B1))(R^(1B2)), —O—R^(1B1), and —S(O)₀₋₂R^(1B1),wherein each R^(1B1) and R^(1B2) is independently hydrogen or methyl,wherein each R^(1A) methyl, cyclopropyl, and morpholinyl is optionallysubstituted with 1 to 4 R^(1C), which can be the same or different, andwherein each R^(1C) is independently methyl, halogen, or cyano. In someembodiments, R¹ is imidazolyl, pyrazolyl, pyridinyl, oxazolyl,isoxazolyl, oxadiazolyl, pyridinonyl, pyrimidinyl, pyridazinyl,benzoisoxazolyl, pyrazolopyridinyl, imidazopyridinyl, orbenzoimidazolyl, each optionally substituted with 1 to 4 substituents,which can be the same or different, each independently selected fromhalogen, cyano, C₁₋₄ alkyl, or C₁₋₄ alkoxy. In some embodiments, R¹ isimidazolyl, pyrazolyl, or pyridinyl, each optionally substituted with 1to 4 substituents, which can be the same or different, eachindependently selected from halogen, cyano, C₁₋₄ alkyl, or C₁₋₄ alkoxy.In some embodiments, R¹ is imidazolyl, pyrazolyl, pyridinyl, oxazolyl,isoxazolyl, oxadiazolyl, pyridinonyl, pyrimidinyl, pyridazinyl,benzoisoxazolyl, pyrazolopyridinyl, imidazopyridinyl, orbenzoimidazolyl, each optionally substituted with 1 to 3 substituents,which can be the same or different, each independently selected from —F,—Cl, —CN, —CH₃, —CHF₂, —CF₃, —OCH₃, —NH₂, —N(CH₃)₂, —SO₂—CH₃,

In some embodiments, R¹ is imidazolyl, pyrazolyl, or pyridinyl, eachoptionally substituted with 1 to 3 substituents, which can be the sameor different, each independently selected from —F, —Cl, —CN, or —CH₃. Insome embodiments, R¹ is

In some embodiments, R¹ is

In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), or (IIn), orpharmaceutically acceptable salt thereof, each R³ is independentlyselected from deuterium, halogen, C₁₋₆ alkyl, C₃₋₆ cycloalkyl,—O—R^(2A1,) and —N(R^(2A1))(R^(2A2)), wherein the C₁₋₆ alkyl isoptionally substituted with 1 to 3 substituents, which can be the sameor different, independently selected from C₁₋₄ alkoxy and halogen, andwherein each R ^(2A1) and R^(2A2) is independently hydrogen or C₁₋₄alkyl optionally substituted with 1 to 3 halogens, which can be the sameor different. In some embodiments, each R³ is independently selectedfrom C₁₋₆ alkyl optionally substituted with 1 to 3 substituents, whichcan be the same or different, independently selected from halogen,cyano, C₁₋₄ alkoxy, and C₃₋₁₀ cycloalkyl. In some embodiments of thecompound of Formula (I), (Ia), (IIa), (IIb), (IIc), (IId), (IIe), (IIf),(IIg), (IIh), (IIi), or (IIn), or pharmaceutically acceptable saltthereof, R³ is —CH₃. In some embodiments of the compound of Formula (I),(Ia), (IIa), (IIb), (IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), or(IIn), or pharmaceutically acceptable salt thereof, R³ is halogen. Insome embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), or (IIn), orpharmaceutically acceptable salt thereof, R³ is —F. In some embodimentsof the compound of Formula (I), (Ia), (IIa), (IIb), (IIc), (IId), (IIe),(IIf), (IIg), (IIh), (IIi), or (IIn), or pharmaceutically acceptablesalt thereof, n is 0, 1, or 2. In some embodiments, n is 0. In someembodiments, n is 1. In some embodiments, n is 2.

In some embodiments of the compound of Formula (I) or (Ia), orpharmaceutically acceptable salt thereof, each Y¹ and Y² isindependently hydrogen, deuterium, or C₁₋₆ alkyl optionally substitutedwith 1 to 3 substituents, which can be the same or different,independently selected from halogen, cyano, C₂₋₃ alkynyl, C₁₋₄ alkoxy,and —C(O)NH—(C₁₋₄H₃₋₉). In some embodiments of the compound of Formula(I), (Ia), (IIa), (IIb), (IIc), (IId), (IIe), (IIf), (IIg), (IIh),(IIi), (IIj), (IIk), (IIl), (IIm), (IIn), or (IIo), or pharmaceuticallyacceptable salt thereof, Y¹ is hydrogen, deuterium, or C₁₋₆ alkyloptionally substituted with 1 to 3 substituents, which can be the sameor different, independently selected from halogen, cyano, C₂₋₃ alkynyl,C₁₋₄ alkoxy, and —C(O)NH—(C₁₋₄H₃₋₉). In some embodiments, Y₁ is C₁₋₄alkyl optionally substituted with 1 to 3 substituents, which can be thesame or different, each independently selected from halogen, cyano, andC₁₋₄ alkoxy, and Y₂ is hydrogen. In some embodiments, Y₁ is methyloptionally substituted with 1 to 3 susbstituents, which can be the sameor different, each independently selected from —F, —Cl, —CN, and —O—CH₃.In some embodiments, Y₁ is —CH₃ or —CH₂F.

In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, Zis C₆₋₁₂ aryl, optionally substituted with 1 to 3 substituents, whichcan be the same or different, each independently selected from halogen,cyano, C₁₋₄ alkyl, C₁₋₄ alkoxy, and C₃₋₆ cycloalkyl, wherein the C₁₋₄alkyl is optionally substituted with 1 to 3 substituents, which can bethe same or different, each independently selected from C₁₋₄ alkoxy andhalogen. In some embodiments, Z is phenyl, optionally substituted with 1to 3 substituents, which can be the same or different, eachindependently selected from halogen and C₁₋₄ alkyl. In some embodiments,Z is phenyl, optionally substituted with 1 to 3 substituents, which canbe the same or different, each independently selected from —F and —Cl.In some embodiments, Z is

In some embodiments, Z is 5 or 6 membered heteroaryl having 1-3heteroatoms independently selected from nitrogen, oxygen, and sulfur,wherein the heteroaryl is optionally substituted with 1 to 3substituents, which can be the same or different, each independentlyselected from halogen and C₁₋₄ alkyl. In some embodiments, Z is pyridyl,optionally substituted with 1 to 3 substituents, which can be the sameor different, each independently selected from —F, —Cl, —Br, and —CH₃.In some embodiments, Z is

In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, Y₁is —CH₃ and Z is

In some embodiments of the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, Y₁is —CH₃ and Z is

In some embodiments the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or pharmaceutically acceptable salt thereof, isselected from the group consisting of:

or a pharmaceutically acceptable salt thereof.

In some embodiments the compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), (IIo), or pharmaceutically acceptable salt thereof, isselected from the group consisting of:

or a pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I), (Ia), or (IIo), orpharmaceutically acceptable salt thereof, is:

or pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I), (Ia), or (IIo), orpharmaceutically acceptable salt thereof, is:

or pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I), (Ia), or (IIo), orpharmaceutically acceptable salt thereof, is:

or pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I), (Ia), or (IIo), orpharmaceutically acceptable salt thereof, is:

or pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I), (Ia), or (IIo), orpharmaceutically acceptable salt thereof, is:

or pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I), (Ia), or (IIo), orpharmaceutically acceptable salt thereof, is:

or pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I), (Ia), or (IIo), orpharmaceutically acceptable salt thereof, is:

or pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I), (Ia), or (IIo), orpharmaceutically acceptable salt thereof, is:

or pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I), (Ia), or (IIo), orpharmaceutically acceptable salt thereof, is:

or pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I), (Ia), or (IIo), orpharmaceutically acceptable salt thereof, is:

or pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I), (Ia), or (IIe), orpharmaceutically acceptable salt thereof, is:

or pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I), (Ia), or (IIe), orpharmaceutically acceptable salt thereof, is:

or pharmaceutically acceptable salt thereof.

In some embodiments, the compound of Formula (I), (Ia), or (IIe), orpharmaceutically acceptable salt thereof, is:

or pharmaceutically acceptable salt thereof.

Pharmaceutical Compositions and Modes of Administration

Furthermore, the present disclosure provides pharmaceutical compositionscomprising at least one compound of the present disclosure, or a prodrugcompound thereof, or a pharmaceutically acceptable salt or solvatethereof as active ingredient together with a pharmaceutically acceptablecarrier.

The pharmaceutical composition of the present disclosure mayadditionally comprise one or more other compounds as active ingredientslike a prodrug compound or other enzyme inhibitors.

The compositions are suitable for oral, rectal, topical, parenteral(including subcutaneous, intramuscular, and intravenous), ocular(ophthalmic), pulmonary (nasal or buccal inhalation) or nasaladministration, although the most suitable route in any given case willdepend on the nature and severity of the conditions being treated and onthe nature of the active ingredient. They may be conveniently presentedin unit dosage form and prepared by any of the methods well-known in theart of pharmacy.

In practical use, the compounds of the present disclosure can becombined as the active ingredient in intimate admixture with apharmaceutical carrier according to conventional pharmaceuticalcompounding techniques. The carrier may take a wide variety of formsdepending on the form of preparation desired for administration, e.g.,oral or parenteral (including intravenous). In preparing thecompositions for oral dosage form, any of the usual pharmaceutical mediamay be employed, such as, for example, water, glycols, oils, alcohols,flavoring agents, preservatives, coloring agents and the like in thecase of oral liquid preparations, such as, for example, suspensions,elixirs and solutions; or carriers such as starches, sugars,microcrystalline cellulose, diluents, granulating agents, lubricants,binders, disintegrating agents and the like in the case of oral solidpreparations such as, for example, powders, hard and soft capsules andtablets, with the solid oral preparations being preferred over theliquid preparations.

Because of their ease of administration, tablets and capsules representthe most advantageous oral dosage unit form in which case solidpharmaceutical carriers are employed. If desired, tablets may be coatedby standard aqueous or non-aqueous techniques. Such compositions andpreparations should contain at least 0.1 percent of active compound. Thepercentage of active compound in these compositions may, of course, bevaried and may conveniently be between about 2 percent to about 60percent of the weight of the unit. The amount of active compound in suchtherapeutically useful compositions is such that an effective dosagewill be obtained. The active compounds can also be administeredintranasally as, for example, liquid drops or spray.

The tablets, pills, capsules, and the like may also contain a bindersuch as gum tragacanth, acacia, corn starch or gelatin; excipients suchas dicalcium phosphate; a disintegrating agent such as corn starch,potato starch, alginic acid; a lubricant such as magnesium stearate; anda sweetening agent such as sucrose, lactose or saccharin. When a dosageunit form is a capsule, it may contain, in addition to materials of theabove type, a liquid carrier such as a fatty oil.

Various other materials may be present as coatings or to modify thephysical form of the dosage unit. For instance, tablets may be coatedwith shellac, sugar or both. A syrup or elixir may contain, in additionto the active ingredient, sucrose as a sweetening agent, methyl andpropylparabens as preservatives, a dye and a flavoring such as cherry ororange flavor.

In some embodiments, the compounds of the present disclosure may also beused as salts with various countercations to yield an orally availableformulation.

The compounds of the present disclosure may also be administeredparenterally. Solutions or suspensions of these active compounds can beprepared in water suitably mixed with a surfactant such ashydroxy-propylcellulose. Dispersions can also be prepared in glycerol,liquid polyethylene glycols and mixtures thereof in oils. Under ordinaryconditions of storage and use, these preparations contain a preservativeto prevent the growth of microorganisms.

The pharmaceutical forms suitable for injectable use include sterileaqueous solutions or dispersions and sterile powders for theextemporaneous preparation of sterile injectable solutions ordispersions. In all cases, the form must be sterile and must be fluid tothe extent that easy syringability exists. It must be stable under theconditions of manufacture and storage and must be preserved against thecontaminating action of microorganisms such as bacteria and fungi. Thecarrier can be a solvent or dispersion medium containing, for example,water, ethanol, polyol (e.g., glycerol, propylene glycol and liquidpolyethylene glycol), suitable mixtures thereof, and vegetable oils.

Any suitable route of administration may be employed for providing amammal, especially a human, with an effective dose of a compound of thepresent disclosure. For example, oral, rectal, topical, parenteral,ocular, pulmonary, nasal, and the like may be employed. Dosage formsinclude tablets, troches, dispersions, suspensions, solutions, capsules,creams, ointments, aerosols, and the like. In some embodiments,compounds of the present disclosure are administered orally.

Kits

Provided herein are also kits that include a compound of the disclosure,or a pharmaceutically acceptable salt, tautomer, stereoisomer, mixtureof stereoisomers, prodrug, or deuterated analog thereof, and suitablepackaging. In one embodiment, a kit further includes instructions foruse. In one aspect, a kit includes a compound of the disclosure, or apharmaceutically acceptable salt, tautomer, stereoisomer, mixture ofstereoisomers, prodrug, or deuterated analog thereof, and a label and/orinstructions for use of the compounds in the treatment of theindications, including the diseases or conditions, described herein.

Provided herein are also articles of manufacture that include a compounddescribed herein or a pharmaceutically acceptable salt, tautomer,stereoisomer, mixture of stereoisomers, prodrug, or deuterated analogthereof in a suitable container. The container may be a vial, jar,ampoule, preloaded syringe, and intravenous bag.

Treatment Methods and Uses

The disclosure further relates to the use of compounds disclosed hereinfor the treatment and/or prophylaxis of diseases and/or conditionsthrough binding of LPAR1 by said compounds. Further, the presentdisclosure relates to the use of said compounds for the preparation of amedicament for the treatment and/or prophylaxis of diseases and/orconditions through binding of LPAR1 by said compounds.

Medicaments as referred to herein may be prepared by conventionalprocesses, including the combination of a compound according to thepresent disclosure and a pharmaceutically acceptable carrier.

In some embodiments, provided herein is a method of treating and/orpreventing an LPAR1-mediated disease or condition in a patient in needthereof, comprising administering to the patient a therapeuticallyeffective amount of a compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), or a pharmaceutically acceptable salt thereof,or a composition comprising a compound of Formula (I), (Ia), (IIa),(IIb), (IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk),(IIl), (IIm), (IIn), or (IIo), or a pharmaceutically acceptable saltthereof.

In some embodiments, the LPAR1-mediated disease or condition includesthose wherein an absolute or relative excess of LPA is present and/orobserved.

In some embodiments, the LPAR1-mediated disease or condition includesfibrosis, wound healing, cancer, pain, respiratory disorders, allergicdisorders, nervous system disorders, cardiovascular disorders, orinflammatory disorders.

In some embodiments, the LPAR1-mediated disease or condition is aninterstitial lung disease (ILD). In some embodiments, the interstitiallung disease (ILD) is nonspecific interstitial pneumonitis (NSIP),sarcoidosis, asbestosis, an ILD related to an occupational exposure,progressive fibrosing ILD, idiopathic interstitial pneumonia (IIP),connective tissue disease-associated interstitial lung disease(CTD-ILD), rheumatoid arthritis-associated ILD, scleroderma-associatedILD, or extrinsic alveolar alveolitis.

In some embodiments, the LPAR1-mediated disease or condition is achronic kidney disease (CKD). In some embodiments, the chronic kidneydisease is complement glomerulopathy, membranous glomerulopathy,polycystic kidney disease, IgA nephropathy, focal segmentalglomerulosclerosis (FSGS), or Alport Syndrome.

In some embodiments, the LPAR1-mediated disease or condition includesfibrosis. In some embodiments, fibrosis includes pulmonary fibrosis,renal fibrosis, hepatic fibrosis, ocular fibrosis, or cardiac fibrosis.

In some embodiments, the LPAR1-mediated disease or condition includespulmonary fibrosis. In some embodiments, pulmonary fibrosis includesidiopathic pulmonary fibrosis (IPF). In some embodiments pulmonaryfibrosis includes Progressive Fibrotic interstitial lung disease(PF-ILD). In some embodiments, pulmonary fibrosis includes pulmonaryfibrosis secondary to systemic inflammatory disease such as rheumatoidarthritis, scleroderma, lupus, cryptogenic fibrosing alveolitis,radiation induced fibrosis, chronic obstructive pulmonary disease(COPD), scleroderma, chronic asthma, silicosis, asbestos inducedpulmonary or pleural fibrosis, acute lung injury and acute respiratorydistress (including bacterial pneumonia induced, trauma induced, viralpneumonia induced, ventilator induced, non-pulmonary sepsis induced, andaspiration induced).

In some embodiments, the LPAR1-mediated disease or condition includesrenal fibrosis. In some embodiments, renal fibrosis includes chronicnephropathies associated with injury/ibrosis (kidney fibrosis), e.g.,glomerulonephritis secondary to systemic inflammatory diseases such aslupus and scleroderma, diabetes, glomerular nephritis, focal segmentalglomerular sclerosis, IgA nephropathy, hypertension, allograft andAlport; gut fibrosis, e.g., scleroderma, and radiation induced gutfibrosis.

In some embodiments, the LPAR1-mediated disease or condition includesliver fibrosis. In some embodiments, liver fibrosis includes livercirrhosis, alcohol induced liver fibrosis, nonalcoholic steatohepatitis(NASH), biliary duct injury, primary biliary cirrhosis, infection orviral induced liver fibrosis (e.g., chronic HCV infection), andautoimmune hepatitis.

In some embodiments, the LPAR1-mediated disease or condition includeshead and neck fibrosis, e.g., radiation induced.

In some embodiments, the LPAR1-mediated disease or condition includescorneal scarring, e.g., due to LASIK (laser-assisted in situkeratomileusis), corneal transplantation, or trabeculectomy. In someembodiments, a compound of Formula (I), (Ia), (IIa), (IIb), (IIc),(IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm),(IIn), or (IIo), or a pharmaceutically acceptable salt thereof, is usedto improve the corneal sensitivity decrease caused by corneal operationssuch as LASIK or cataract operation, corneal sensitivity decrease causedby corneal degeneration, and dry eye symptom caused thereby. In someembodiments, a compound of Formula (I), (Ia), (IIa), (Ilb), (IIc),(IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm),(IIn), or (IIo), or a pharmaceutically acceptable salt thereof, is usedin the treatment or prevention of ocular inflammation and allergicconjunctivitis, vernal keratoconjunctivitis, and papillaryconjunctivitis. In some embodiments, a compound of Formula (I), (Ia),(IIa), (IIb), (IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj),(IIk), (IIl), (IIm), (IIn), or (IIo), or a pharmaceutically acceptablesalt thereof, is used in the treatment or prevention of Sjogren diseaseor inflammatory disease with dry eyes.

In some embodiments, the LPAR1-mediated disease or condition includesanother fibrotic condition, such as hypertrophic scarring and keloids,e.g., burn induced or surgical, sarcoidosis, scleroderma, spinal cordinjury/fibrosis, myelofibrosis, vascular restenosis, atherosclerosis,arteriosclerosis, Wegener's granulomatosis, mixed connective tissuedisease, and Peyronie's disease.

In some embodiments, the LPAR1-mediated disease or condition includespain. In some embodiments, pain includes neuropathic pain. In someembodiments, pain includes acute pain. In some embodiments, painincludes chronic pain.

In some embodiments, the LPAR1-mediated disease or condition includescancer. In some embodiments, cancer includes ovarian cancer, coloncancer, prostate cancer, breast cancer, melanoma, head and neck cancer,bowel cancer (colorectal cancer), and thyroid cancer. In someembodiments, cancer includes solid tumors, such as (such as those of thebladder, bowel, brain, breast, endometrium, heart, kidney, lung,lymphatic tissue (lymphoma), ovary, pancreas or other endocrine organ(thyroid), prostate, skin (melanoma or basal cell cancer) orhematological tumors (such as the leukemias) at any stage of the diseasewith or without metastases. In some embodiments, cancer includes, acutelymphoblastic leukemia, acute myeloid leukemia, adrenocorticalcarcinoma, anal cancer, appendix cancer, astrocytomas, atypicalteratoid/rhabdoid tumor, basal cell carcinoma, bile duct cancer, bladdercancer, bone cancer (osteosarcoma and malignant fibrous histiocytoma),brain stem glioma, brain tumors, brain and spinal cord tumors, breastcancer, bronchial tumors, Burkitt lymphoma, cervical cancer, chroniclymphocytic leukemia, chronic myelogenous leukemia, colon cancer,colorectal cancer, craniopharyngioma, cutaneous T-Cell lymphoma,embryonal tumors, endometrial cancer, ependymoblastoma, ependymoma,esophageal cancer, ewing sarcoma family of tumors, eye cancer,retinoblastoma, gallbladder cancer, gastric (stomach) cancer,gastrointestinal carcinoid tumor, gastrointestinal stromal tumor (GIST),gastrointestinal stromal cell tumor, germ cell tumor, glioma, hairy cellleukemia, head and neck cancer, hepatocellular (liver) cancer, Hodgkinlymphoma, hypopharyngeal cancer, intraocular melanoma, islet cell tumors(endocrine pancreas), Kaposi sarcoma, kidney cancer, Langerhans cellhistiocytosis, laryngeal cancer, leukemia, Acute lymphoblastic leukemia,acute myeloid leukemia, chronic lymphocytic leukemia, chronicmyelogenous leukemia, hair) cell leukemia, liver cancer, non-small celllung cancer, small cell lung cancer, Burkitt lymphoma, cutaneous T-celllymphoma, Hodgkin lymphoma, non-Hodgkin lymphoma, lymphoma, Waldenstrommacroglobulinemia, medulloblastoma, medulloepithelioma, melanoma,mesothelioma, mouth cancer, chronic myelogenous leukemia, myeloidleukemia, multiple myeloma, nasopharyngeal cancer, neuroblastoma,non-Hodgkin lymphoma, non-small cell lung cancer, oral cancer,oropharyngeal cancer, osteosarcoma, malignant fibrous histiocytoma ofbone, ovarian cancer, ovarian epithelial cancer, ovarian germ celltumor, ovarian low malignant potential tumor, pancreatic cancer,papillomatosis, parathyroid cancer, penile cancer, pharyngeal cancer,pineal parenchymal tumors of intermediate differentiation, pineoblastomaand supratentorial primitive neuroectodermal tumors, pituitary tumor,plasma cell neoplasm/multiple myeloma, pleuropulmonary blastema, primarycentral nervous system lymphoma, prostate cancer, rectal cancer, renalcell (kidney) cancer, retinoblastoma, rhabdomyosarcoma, salivary glandcancer, sarcoma, Ewing sarcoma family of tumors, sarcoma, kaposi, Sezarysyndrome, skin cancer, small cell Lung cancer, small intestine cancer,soft tissue sarcoma, squamous cell carcinoma, stomach (gastric) cancer,supratentorial primitive, neuroectodermal tumors, T-cell lymphoma,testicular cancer, throat cancer, thymoma and thymic carcinoma, thyroidcancer, urethral cancer, uterine cancer, uterine sarcoma, vaginalcancer, vulvar cancer, Waldenstrom macroglobulinemia, and Wilms tumor.

In some embodiments, the LPAR1-mediated disease or condition includes arespiratory or allergic disorder. In some embodiments, the respiratoryor allergic disorder includes asthma, peribronchiolar fibrosis,obliterative bronchiolitis, and chronic obstructive pulmonary disease(COPD). In some embodiments, the COPD includes chronic bronchitis oremphysema, pulmonary hypertension, interstitial lung fibrosis and/orairway inflammation, and cystic fibrosis. In some embodiments, therespiratory disease includes adult respiratory distress syndrome andallergic (extrinsic) asthma, non-allergic (intrinsic) asthma, acutesevere asthma, chronic asthma, clinical asthma, nocturnal asthma,allergen-induced asthma, aspirin-sensitive asthma, exercise-inducedasthma, isocapnic hyperventilation, child-onset asthma, adult-onsetasthma, cough-variant asthma, occupational asthma, steroid-resistantasthma, seasonal asthma, seasonal allergic rhinitis, perennial allergicrhinitis, and hypoxia.

In some embodiments, the LPAR1-mediated disease or condition includes anervous system disorder. In some embodiments, the nervous systemdisorder includes Alzheimer's Disease, cerebral edema, cerebralischemia, stroke, multiple sclerosis, neuropathies, Parkinson's Disease,a nervous condition found after blunt or surgical trauma (includingpost-surgical cognitive dysfunction and spinal cord or brim steminjury), as well as the neurological aspects of disorders such asdegenerative disk disease and sciatica.

In some embodiments, the LPAR1-mediated disease or condition includes acardiovascular disorder. In some embodiments, the cardiovasculardisorder includes arrhythmia. (atrial or ventricular or both);atherosclerosis and its sequelae; angina; cardiac rhythm disturbances;myocardial ischemia; myocardial infarction; cardiac or vascularaneurysm; vasculitis; stroke; peripheral obstructive arteriopathy of alimb, an organ, or a tissue; reperfusion injury following ischemia ofthe brain, heart or other organ or tissue; endotoxic, surgical, ortraumatic shock; hypertension; valvular heart disease; heart failure;abnormal blood pressure; shock; vasoconstriction (including thatassociated with migraines); vascular abnormality, and a cardiovascularinsufficiency limited to a single organ or tissue.

In some embodiments, the LPAR1-mediated disease or condition includeslung fibrosis, kidney fibrosis, liver fibrosis, scarring, asthma,rhinitis, chronic obstructive pulmonary disease (COPD), pulmonaryhypertension, interstitial lung fibrosis, arthritis, allergy, psoriasis,inflammatory bowel disease, adult respiratory distress syndrome,myocardial infarction, aneurysm, stroke, cancer, pain, proliferativedisorders and inflammatory conditions.

In some embodiments, the LPAR1-mediated disease or condition is a liverdisease. In some embodiments, the liver disease is hepatitis C, livercancer, familial combined hyperlipidemia, non-alcoholic fatty liverdisease (NAFLD), progressive familial intrahepatic cholestasis, primarybiliary cirrhosis (PBC), or (PSC). In some embodiments, the liverdisease is PSC. In some embodiments the liver disease comprises portalhypertension. In some embodiments, liver cancer comprises hepatocellularcarcinoma (HCC), cholangiocarcinoma, angiosarcoma, or hemangiosarcoma.In some embodiments, liver cancer comprises HCC. In some embodiments,NAFLD comprises steatosis. In some embodiments, NAFLD comprises NASH. Insome embodiments, NAFLD or NASH comprises liver fibrosis. In someembodiments, NAFLD or NASH comprises liver cirrhosis. In someembodiments, the NAFLD or NASH comprises compensated liver cirrhosis. Insome embodiments, the NAFLD or NASH comprises decompensated liverfibrosis. In some embodiments, the NAFLD comprises HCC. In someembodiments, the liver disease is NASH.

In some embodiments, provided herein is a method of treating and/orpreventing NAFLD or NASH in a patient in need thereof, comprisingadministering to the patient a therapeutically effective amount of acompound of Formula (I), (Ia), (IIa), (IIb), (IIc), (IId), (IIe), (IIf),(IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm), (IIn), or (IIo), orpharmaceutically acceptable salt thereof, or a composition comprising acompound of Formula (I), (Ia), (IIa), (IIb), (IIc), (IId), (IIe), (IIf),(IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm), (IIn), or (IIo), orpharmaceutically acceptable salt thereof. In some embodiments, NAFLD orNASH comprise liver fibrosis. In some embodiments, NAFLD or NASHcomprise liver cirrhosis. In some embodiments, liver cirrhosis iscompensated liver cirrhosis. In some embodiments, liver cirrhosis isdecompensated liver cirrhosis. In some embodiments NAFLD or NASHcomprise HCC.

In some embodiments, provided herein is a method of preventing a liverdisease or condition in a patient in need thereof, comprisingadministering to the patient a therapeutically effective amount of acompound of Formula (I), (Ia), (IIa), (IIb), (IIc), (IId), (IIe), (IIf),(IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm), (IIn), or (IIo), orpharmaceutically acceptable salt thereof, or a composition comprising acompound of Formula (I), (Ia), (IIa), (IIb), (IIc), (IId), (IIe), (IIf),(IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm), (IIn), or (IIo), orpharmaceutically acceptable salt thereof. In some embodiments, the liverdisease or condition is liver fibrosis. In some embodiments, the liverdisease or condition is liver cirrhosis. In some embodiments, livercirrhosis is compensated liver cirrhosis. In some embodiments, livercirrhosis is decompensated liver cirrhosis. In some embodiments, theliver disease or condition is HCC.

In some embodiments, the present disclosure relates to the use ofcompounds according to Formula (I), (Ia), (IIa), (IIb), (IIc), (IId),(IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm), (IIn), or(IIo), or pharmaceutically acceptable salts thereof, in the preparationof a medicament for the prophylaxis and/or treatment of anLPAR1-mediated disease or condition disclosed herein.

Dosage

The effective dosage of active ingredient employed may vary depending onthe particular compound employed, the mode of administration, thecondition being treated and the severity of the condition being treated.Such dosage may be ascertained readily by a person skilled in the art.

When treating or preventing an LPAR1 mediated disease or condition forwhich compounds of the present disclosure are indicated, generallysatisfactory results are obtained when the compounds of the presentdisclosure are administered at a daily dosage of from about 0.1milligram to about 300 milligram per kilogram of animal body weight. Insome embodiments, the compounds of the present disclosure are given as asingle daily dose or in divided doses two to six times a day, or insustained release form. For most large mammals, the total daily dosageis from about 1 milligram to about 1000 milligrams, or from about 1milligram to about 50 milligrams. In the case of a 70 kg adult human,the total daily dose will generally be from about 0.1 milligrams toabout 200 milligrams. This dosage regimen may be adjusted to provide theoptimal therapeutic response. In some embodiments, the total dailydosage is from about 1 milligram to about 900 milligrams, about 1milligram to about 800 milligrams, about 1 milligram to about 700milligrams, about 1 milligram to about 600 milligrams, about 1 milligramto about 400 milligrams, about 1 milligram to about 300 milligrams,about 1 milligram to about 200 milligrams, about 1 milligram to about100 milligrams, about 1 milligram to about 50 milligrams, about 1milligram to about 20 milligram, or about 1 milligram to about 10milligrams.

The compounds of the present application or the compositions thereof maybe administered once, twice, three, or four times daily, using anysuitable mode described above. Also, administration or treatment withthe compounds may be continued for a number of days; for example,commonly treatment would continue for at least 7 days, 14 days, or 28days, for one cycle of treatment. Treatment cycles are frequentlyalternated with resting periods of about 1 to 28 days, commonly about 7days or about 14 days, between cycles. The treatment cycles, in otherembodiments, may also be continuous.

In some embodiments, the methods provided herein comprise administeringto the subject an initial daily dose of about 1 to 800 mg of a compounddescribed herein and increasing the dose by increments until clinicalefficacy is achieved. Increments of about 5, 10, 25, 50, or 100 mg canbe used to increase the dose. The dosage can be increased daily, everyother day, twice per week, or once per week.

Combinations

In some embodiments, a compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), provided herein, or pharmaceutically acceptablesalt thereof, is administered in combination with one or more additionaltherapeutic agents to treat or prevent a disease or condition disclosedherein. In some embodiments, the one or more additional therapeuticagents are one, two, three, or four additional therapeutic agents. Insome embodiments, the one or more additional therapeutic agents are oneadditional therapeutic agent. In some embodiments, the one or moreadditional therapeutic agents are two additional therapeutic agents. Insome embodiments, the one or more additional therapeutic agents arethree additional therapeutic agents. In some embodiments, the one ormore additional therapeutic agents are four additional therapeuticagents.

In some embodiments, the pharmaceutical compositions provided hereinhave a compound of Formula (I), (Ia), (IIa), (IIb), (IIc), (IId), (IIe),(IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl), (IIm), (IIn), or (IIo),provided herein, or pharmaceutically acceptable salt thereof, and one ormore additional therapeutic agents. In some embodiments, the one or moreadditional therapeutic agents are one, two, three, or four additionaltherapeutic agents. In some embodiments, the one or more additionaltherapeutic agents are one additional therapeutic agent. In someembodiments, the one or more additional therapeutic agents are twoadditional therapeutic agents. In some embodiments, the one or moreadditional therapeutic agents are three additional therapeutic agents.In some embodiments, the one or more additional therapeutic agents arefour additional therapeutic agents.

In some embodiments, the one or more additional therapeutic agents areselected from a(n) angiotensin converting enzyme (ACE) inhibitor,Adenosine A3 receptor agonist, Adiponectin receptor agonist, AKT proteinkinase inhibitor, AMP kinase activator, AMP-activated protein kinase(AMPK) activator, Amylin receptor agonist, Angiotensin II AT-1 receptorantagonist, Androgen receptor agonist, Apoptosis signal-regulatingkinase 1 (ASK1) inhibitor, ATP citrate lyase inhibitor, ApolipoproteinC3 (APOC3) antagonist, Autophagy protein modulator, Autotaxininhibitors, Axl tyrosine kinase receptor inhibitor, Bax proteinstimulator, Bioactive lipid, Calcitonin agonist, Cannabinoid receptormodulator, Caspase inhibitor, Caspase-3 stimulator, Cathepsin inhibitor(e.g., cathepsin B inhibitor), Caveolin 1 inhibitor, CCR2 chemokineantagonist, CCR3 chemokine antagonist, CCR5 chemokine antagonist, CD3antagonist, Chloride channel stimulator, cholesterol solubilizer, CNR1inhibitor, Cyclin D1 inhibitor, Cytochrome P450 7A1 inhibitor,Cytochrome P450 2E1 (CYP2E1) inhibitor, Diacylglycerol O acyltransferase1 inhibitor (DGAT1) inhibitor, Diacylglycerol O acyltransferase 1inhibitor (DGAT2) inhibitor, CXCR4 chemokine antagonist, Dipeptidylpeptidase IV inhibitor, Endosialin modulator, Endothelial nitric oxidesynthase stimulator, Eotaxin ligand inhibitor, Extracellular matrixprotein modulator, Farnesoid X receptor agonist, Fatty acid synthaseinhibitors, FGF1 receptor agonist, Fibroblast activation protein (FAP)inhibitor, Fibroblast growth factor receptor ligands (e.g., FGF-15,FGF-19, FGF-21), Fish oil, Galectin-3 inhibitor, Glucagon receptoragonist, Glucagon-like peptide 1 receptor agonist, Glucocorticoidreceptor antagonist, Glucose 6-phosphate 1-dehydrogenase inhibitor,Glutaminase inhibitor, Glutathione precursor, G-protein coupled bileacid receptor 1 agonist, G-protein coupled receptor 84 antagonist,Hedgehog (Hh) modulator, Hepatitis C virus NS3 protease inhibitor,Hepatocyte nuclear factor 4 alpha modulator (HNF4A), Hepatocyte growthfactor modulator, Histone deacetylase inhibitor, HMG CoA reductaseinhibitor, 11β-Hydroxysteroid dehydrogenase (11β-HSD1) inhibitor,Hypoxia inducible factor-2 alpha inhibitor, IL-1β antagonist, IL-6receptor agonist, IL-10 agonist, IL-11 antagonist, IL-17 antagonist,Ileal sodium bile acid cotransporter inhibitor, Insulin sensitizer,Insulin ligand agonist, Insulin receptor agonist, integrin modulator,Integrin antagonist intereukin-1 receptor-associated kinase 4 (IRAK4)inhibitor, Jak2 tyrosine kinase inhibitor, Ketohexokinase (KHK)inhibitors, Klotho beta stimulator, leptin, leptin analog,5-Lipoxygenase inhibitor, Lipoprotein lipase inhibitor, Liver Xreceptor, LPL gene stimulator, Lysophosphatidate-1 receptor (LPAR-1)antagonist, Lysyl oxidase homolog 2 (LOXL2) inhibitor, LXR inverseagonist, Macrophage mannose receptor 1 modulator, Matrixmetalloproteinase (MMPs) inhibitor, MCH receptor-1 antagonist, MEKK-5protein kinase inhibitor, Membrane copper amine oxidase (VAP-1)inhibitor, Methionine aminopeptidase-2 inhibitor, Methyl CpG bindingprotein 2 modulator, MicroRNA-132 (miR-132) antagonist,MicroRNA-21(miR-21) inhibitor, Mitochondrial uncoupler, Mixed lineagekinase-3 inhibitor, Myelin basic protein stimulator, NACHT LRR PYDdomain protein 3 (NLRP3) inhibitor, NAD-dependent deacetylase sirtuin-1stimulator, NADPH oxidase inhibitor (NOX), Nicotinic acid receptor 1agonist, P2X7 purinoceptor modulator, P2Y13 purinoceptor stimulator, PDE3 inhibitor, PDE 4 inhibitor, PDE 5 inhibitor, PDGF receptor betamodulator, Peptidyl-prolyl cis-trans isomerase A inhibitor,Phenylalanine hydroxylase stimulator, Phospholipase C inhibitor, PPARalpha agonist, PPAR gamma agonist, PPAR delta agonist, PPAR gammamodulator, PPAR alpha/delta agonist, PPAR alpha/gamma/delta agonist,Protease-activated receptor-2 antagonist, Protein kinase modulator, Rhoassociated protein kinase 2 (ROCK2) inhibitor, Snitrosoglutathionereductase (GSNOR) enzyme inhibitor, Sodium glucose transporter-2 (SGLT2)inhibitor, SREBP transcription factor inhibitor, STAT-1 inhibitor,STAT-3 modulator, Stearoyl CoA desaturase-1 inhibitor,Snitrosoglutathione reductase (GSNOR) enzyme inhibitor, Suppressor ofcytokine signalling-1 stimulator, Suppressor of cytokine signalling-3stimulator, Spleen tyorosine kinase (SYK) inhibitor, Transforming growthfactor β (TGF-β), TGF-β antagonist (e.g., TGF-β1 antagonist, TGF-β2antagonist, TGF-β3 antagonist, latent TGF β complex modulator), TGF-βreceptor antagonist, Transforming growth factor β activated Kinase 1(TAK1), Thyroid hormone receptor beta agonist, Toll-like receptor(TLR)-4 antagonist, Transglutaminase inhibitor, Tumor necrosis factoralpha (TNFα) ligand inhibitor, Tumor Progression Locus 2 (Tpl2) kinaseinhibitor, Tyrosine kinase receptor modulator, GPCR modulator, nuclearhormone receptor modulator, WNT modulators, YAP/TAZ modulator, andZonulin inhibitor.

Non-limiting examples of the one or more additional therapeutic agentsinclude:

ACE inhibitors, such as enalapril;

Acetyl CoA carboxylase (ACC) inhibitors, such as NDI-010976(firsocostat), DRM-01, gemcabene, PF-05175157, QLT-091382 orPF-05221304;

Acetyl CoA carboxylase/Diacylglycerol O acyltransferase 2 inhibitors,such as PF-07055341;

Acetaldehyde dehydrogenase inhibitors, such as ADX-629;

Adenosine receptor agonists, such as CF-102 (namodenoson), CF-101,CF-502, or CGS21680;

Adiponectin receptor agonists, such as ADP-355 or ADP-399;

Amylin/calcitonin receptor agonists, such as KBP-042 or KBP-089;

AMP activated protein kinase stimulators, such as PXL-770 or O-304;

AMP kinase activators/ATP citrate lyase inhibitors, such as as bempedoicacid (ETC-1002, ESP-55016);

AMP activated protein kinase/Endothelial nitric oxidesynthase/NAD-dependent deacetylase sirtuin-1 stimulators, such asNS-0200 (leucine+metformin+sildenafil);

Androgen receptor agonists, such as LPCN-1144;

Angiotensin II AT-1 receptor antagonists, such as irbesartan;

Angiopoietin-related protein-3 inhibitors, such as IONIS-ANGPTL3-LRx;

Autotaxin inhibitors, such as PAT-505, PAT-048, GLPG-1690, X-165,PF-8380, AM-063, or BBT-877;

Axl tyrosine kinase receptor inhibitors, such as bemcentinib (BGB-324,R-428);

Bax protein stimulators, such as CBL-514;

Bioactive lipids, such as DS-102;

Cannabinoid receptor type 1 (CNR1) inhibitors, such as namacizumab,GWP-42004, REV-200, or CRB-4001;

Caspase inhibitors, such as emricasan;

Pan cathepsin B inhibitors, such as VBY-376;

Pan cathepsin inhibitors, such as VBY-825;

CCR2/CCR5 chemokine antagonists, such as cenicriviroc, maraviroc,CCX-872, or WXSH-0213;

CCR2 chemokine antagonists, such as propagermanium;

CCR2 chemokine/Angiotensin II AT-1 receptor antagonists, such asDMX-200, or DMX-250;

CCR2/CCR5 chemokine antagonists and FXR agonists, such as LJC-242(tropifexor+cenivriviroc); CCR3 chemokine antagonists, such asbertilimumab;

Chloride channel stimulators, such as cobiprostone, or lubiprostone;

CD3 antagonists, such as NI-0401 (foralumab);

CXCR4 chemokine antagonists, such as AD-214;

Diglyceride acyltransferase 1 (DGAT1) inhibitors, such as GSK-3008356;

Diacylglycerol O acyltransferase 1 (DGAT1)/Cytochrome P450 2E1inhibitors (CYP2E1), such as SNP-610;

Diglyceride acyltransferase 2 (DGAT2) inhibitors, such as IONIS-DGAT2Rx,or PF-06865571;

Dipeptidyl peptidase IV inhibitors, such as linagliptin or evogliptin;

Eotaxin ligand inhibitors, such as bertilimumab or CM-101;

Extracellular matrix protein modulators, such as CNX-024;

Farnesoid X receptor (FXR) agonists, such as AGN-242266, AGN-242256,EP-024297, RDX-023, BWL-200, AKN-083, EDP-305, GNF-5120, GS-9674,LMB-763, obeticholic acid, Px-102, Px-103, M790, M780, M450, M-480,MET-409, PX20606, EYP-001, TERN-101, TC-100, INT-2228;

Farnesoid X receptor (FXR)/G-protein coupled bile acid receptor 1 (TGR5)agonists, such as INT-767;

Fatty acid synthase inhibitors, such as TVB-2640;

FGF receptor agonists/Klotho beta stimulators, such as BFKB-8488A(RG-7992);

Fibroblast growth factor 19 (rhFGF19)/cytochrome P450 (CYP)7A1inhibitors, such as NGM-282;

Fibroblast growth factor 21 (FGF-21) ligand, such as BMS-986171,BIO89-100, B-1344, or BMS-986036;

Fibroblast growth factor 21 (FGF-21)/glucagon like peptide 1 (GLP-1)agonists, such as YH-25723 (YH-25724; YH-22241) or AKR-001;

Fish oil compositions, such as icosapent ethyl (Vascepa®);

Galectin-3 inhibitors, such as GR-MD-02, GB-1107 (Gal-300), or GB1211(Gal-400);

Glucagon-like peptide 1 receptor (GLP1R) agonists, such as AC-3174,liraglutide, cotadutide (MEDI-0382), exenatide, SAR-425899, LY-3305677,HM-15211, YH-25723, YH-GLP1, RPC-8844, PB-718, or semaglutide;

Glucocorticoid receptor antagonists, such as CORT-118335 (miricorilant);

Glucose 6-phosphate 1-dehydrogenase inhibitors, such as ST001;

G-protein coupled bile acid receptor 1 (TGR5) agonists, such as RDX-009or INT-777;

Heat shock protein 47 (HSP47) inhibitors, such as ND-L02-s0201;

HMG CoA reductase inhibitors, such as atorvastatin, fluvastatin,pitavastatin, pravastatin, rosuvastatin, or simvastatin;

Hypoxia inducible factor-2 alpha inhibitors, such as PT-2567;

IL-10 agonists, such as peg-ilodecakin;

Ileal sodium bile acid cotransporter inhibitors, such as odevixibat(A-4250), volixibat potassium ethanolate hydrate (SHP-262), GSK2330672,CJ-14199, or elobixibat (A-3309);

Insulin sensitizers, such as, KBP-042, MSDC-0602K, MSDC-5514, Px-102,RG-125 (AZD4076), VVP-100X, CB-4211, or ETI-101;

Insulin ligand/dsInsulin receptor agonists, such as ORMD-0801;

Integrin antagonists, such as IDL-2965;

IL-6 receptor agonists, such as KM-2702;

Ketohexokinase (KHK) inhibitors, such as PF-06835919;

beta Klotho (KLB)-FGF1c agonist, such as MK-3655 (NGM-313);

5-Lipoxygenase inhibitors, such as tipelukast (MN-001), DS-102 (AF-102);

Lipoprotein lipase inhibitors, such as CAT-2003;

LPL gene stimulators, such as alipogene tiparvovec;

Liver X receptor (LXR) modulators, such as PX-L603, PX-L493, BMS-852927,T-0901317, GW-3965, or SR-9238;

Lysophosphatidate-1 receptor antagonists, such as BMT-053011, UD-009(CP-2090), AR-479, ITMN-10534, BMS-986020, or KI-16198;

Lysyl oxidase homolog 2 inhibitors, such as simtuzumab or PXS-5382A(PXS-5338);

Macrophage mannose receptor 1 modulators, such as tilmanocept-Cy3(technetium Tc 99m tilmanocept);

Membrane copper amine oxidase (VAP-1) inhibitors, such as TERN-201;

MEKK-5 protein kinase (ASK-1) inhibitors, such as GS-4997, SRT-015, orGS-444217, GST-HG-151;

MCH receptor-1 antagonists, such as CSTI-100 (ALB-127158);

Methionine aminopeptidase-2 inhibitors, such as ZGN-839, ZGN-839, orZN-1345;

Methyl CpG binding protein 2 modulators, such as mercaptamine;

Mitochondrial uncouplers, such as 2,4-dinitrophenol or HU6;

Mixed lineage kinase-3 inhibitors, such as URMC-099-C;

Myelin basic protein stimulators, such as olesoxime;

NADPH oxidase 1/4 inhibitors, such as GKT-831 or APX-311;

Nicotinic acid receptor 1 agonists, such as ARI-3037MO;

Nitazoxinide;

NACHT LRR PYD domain protein 3 (NLRP3) inhibitors, such asKDDF-201406-03, NBC-6, IFM-514, or JT-194 (JT-349);

Nuclear receptor modulators, such as DUR-928 (DV-928);

P2X7 purinoceptor modulators, such as SGM-1019;

P2Y13 purinoceptor stimulators, such as CER-209;

PDE 3/4 inhibitors, such as tipelukast (MN-001);

PDE 5 inhibitors, such as sildenafil or MSTM-102;

PDGF receptor beta modulators, such as BOT-191 or BOT-509;

Peptidyl-prolyl cis-trans isomerase inhibitors, such as CRV-431(CPI-432-32), NVP-018, or NV-556 (NVP-025);

Phenylalanine hydroxylase stimulators, such as HepaStem;

PPAR agonists (including PPAR alpha agonists, PPAR alpha/delta agonists,PPAR alpha/delta/gamma agonists, PPAR delta agonists), such aselafibranor (GFT-505), MBX-8025, deuterated pioglitazone R-enantiomer,pioglitazone, DRX-065, saroglitazar, or IVA-337; PPAR alpha agonists,such as aluminum clofibrate, bezafibrate, ciprofibrate, cholinefenofibrate, clinofibrate, clofibrate, clofibride, fenofibrate,gemfibrozil, pemafibrate, ronifibrate, simfibrate, an omega-3 fatty acid(fish oil, e.g., icosapent ethyl (Vascepa®), or docosahexaenoic acid),pirinixic acid, GW409544, AZ 242, LY518674, NS-220, AVE8134, BMS-711939,aleglitazar, muraglitzar, or saroglitazar;

PPAR alpha/delta agonists such as elafibranor;

PPAR alpha/delta/gamma agonists such as lanifibranor;

PPAR delta agonists such as seladelpar;

Protease-activated receptor-2 antagonists, such as PZ-235;

Protein kinase modulators, such as CNX-014;

Rho associated protein kinase (ROCK) inhibitors, such as REDX-10178(REDX-10325) or KD-025;

Semicarbazide-Sensitive Amine Oxidase/Vascular Adhesion Protein-1(SSAO/VAP-1) Inhibitors, such as PXS-4728A;

S-nitrosoglutathione reductase (GSNOR) enzyme inhibitors, such asSL-891;

Sodium glucose transporter-2 (SGLT2) inhibitors, such as ipragliflozin,remogliflozin etabonate, ertugliflozin, dapagliflozin, tofogliflozin, orsotagliflozin;

SREBP transcription factor inhibitors, such as CAT-2003 or MDV-4463;

Stearoyl CoA desaturase-1 inhibitors, such as aramchol;

Thyroid hormone receptor (THR) beta agonists, such as resmetriom(MGL-3196), MGL-3745, or VK-2809;

TLR-2/TLR-4 antagonists, such as VB-201 (CI-201);

TLR-4 antagonists, such as JKB-121;

Tyrosine kinase receptor modulators, such as CNX-025 or GFE-2137(repurposed nitazoxanide);

GPCR modulators, such as CNX-023;

Nuclear hormone receptor modulators, such as Px-102;

Xanthine oxidase/Urate anion exchanger 1 (URAT1) inhibitors, such asRLBN-1001, RLBN-1127; and

Zonulin Inhibitors, such as lorazotide acetate (INN-202).

Additional non-limiting examples of the one or more additionaltherapeutic agents include:

-   -   ACE inhibitors, such as, benazepril, imidapril;    -   Adenosine A3 receptor antagonists, such as FM-101;    -   Adropin stimulators, such as RBT-2;    -   Albumin modulators, such as SYNT-002;    -   Aldosterone/Mineralocorticoid receptor antagonists, such as        MT-3995;    -   Allogeneic bone marrow-derived mesenchymal stromal cell therapy,        such as ORBCEL-M;    -   Allogenic expanded adipose-derived stem cell therapy, such as        Elixcyte™;    -   AMP activated protein kinase stimulator/Proprotein convertase        PC9 inhibitors, such as O-304;    -   AMP activated protein kinase stimulators, such as DZCY-01,        MK-8722, PXL-770;    -   Angiotensin II AT-1 receptor/CCR2 chemokine antagonists, such as        DMX-200;    -   Angiotensin II AT-2 receptor agonists, such as MOR-107,        irbesartan;    -   Angiotensin II receptor antagonists, such as losartan;    -   Angiotensinogen ligand inhibitors, such as ALN-AGT;    -   anti-C1 antibodies, such as BIVV-009 (sutimlimab);    -   anti-CB1 antibodies, such as GFB-024;    -   anti-CX3CR1 nanobodies, such as BI-655088;    -   anti-IL-6 antibodies, such as COR-001;    -   anti-VEGF-B antibodies, such as CSL-346;    -   APOA1 gene stimulators/Bromodomain containing protein        2/Bromodomain containing protein 4 inhibitors, such as        apabetalone;    -   Bone morphogenetic protein-7 ligand modulators, such as BMP-7;    -   Calcium channel inhibitors, such as TBN (xiaotongqin);    -   Cannabinoid CB1 receptor antagonists, such as JNJ-2463;    -   CB1 inverse agonists, such as CRB-4001;    -   Chymase inhibitors, such as fulacimstat (BAY-1142524);    -   Cyclooxygenase 1 inhibitors, such as GLY-230;    -   Cyclooxygenase 2/Epoxide hydrolase inhibitors, such as        COX-2/soluble epoxide hydrolase;    -   Cytochrome P450 11B2 inhibitors, such as aldosterone synthase        inhibitors;    -   Ectonucleotide pyrophosphatase-PDE-2 inhibitors, such as        BLD-0409;    -   Endothelin ET-A/Endothelin ET-B receptor antagonists, such as        aprocitentan;    -   Enteropeptidase inhibitors, such as SCO-792;    -   Erythropoietin receptor antagonists, such as EPO-018B;    -   Farnesoid X receptor agonists, such as LMB-763;    -   FGF/PDGF/beta receptor antagonist/p38 MAP kinase inhibitors,        such as pirfenidone;    -   GHR/IGF1 gene inhibitors, such as atesidorsen sodium;    -   GPR40 agonist/GPR84 antagonists, such as PBI-4050;    -   G-protein beta subunit inhibitors, such as galleon;    -   G-protein coupled receptor 84 modulators, such as PBI-4425;    -   Growth hormone ligand/Growth hormone receptor agonist, such as        Jintropin AQ™;    -   Growth hormone receptor agonists, such as LAT-8881;    -   Guanylate cyclase receptor agonist/Guanylate cyclase        stimulators, such as praliciguat;    -   Guanylate cyclase stimulators, such as MRL-001, runcaciguat;    -   Heme oxygenase 1 modulators, such as RBT-1;    -   HIF prolyl hydroxylase inhibitors, such as TRGX-154;    -   Insulin sensitizer/Kallikrein 1 modulators, such as DM-199;    -   Integrin alpha-V/beta-3 antagonists, such as VPI-2690B;    -   Interleukin 33 ligand inhibitors, such as MEDI-3506;    -   Kelch like ECH associated protein 1 modulator/Nuclear erythroid        2-related factor 2 stimulators, such as SFX-01;    -   LDHA gene inhibitors, such as nedosiran;    -   5-Lipoxygenase activating protein inhibitors, such as AZD-5718;    -   Lysophosphatidate-1 receptor antagonists, such as BMS-002,        EPGN-696;    -   Matrix extracell phosphoglycoprotein modulator/Phosphatonin        receptor agonist, such as TPX-200;    -   MEKK-5 protein kinase inhibitors, such as selonsertib;    -   Membrane copper amine oxidase inhibitors, such as UD-014;    -   Midkine ligand inhibitors, such as CAB-101;    -   Mineralocorticoid receptor antagonists, such as AZD-9977,        esaxerenone, finerenone, KBP-5074;    -   Myosin 2 inhibitor, such as DeciMab™;    -   NADPH oxidase 1 inhibitors/NADPH oxidase 4 inhibitors, such as        setanaxib;    -   NADPH oxidase inhibitors, such as APX-115;    -   NK1 receptor antagonist/Opioid receptor kappa agonist/Opioid        receptor mu antagonist, such as AV-104;    -   Nuclear erythroid 2-related factor 2 stimulator/TGF beta ligand        inhibitors, such as CU01-1001;    -   Nuclear factor kappa B inhibitors, such as mefunidone,        bardoxolone methyl (NSC-713200);    -   PDE 4 inhibitors, such as ART-648, PCS-499;    -   PDGF receptor beta modulators, such as BOT-191;    -   PDGF/VEGF receptor antagonists, such as ANG-3070;    -   PR84 antagonist/GPR40 (FFAR1)/GPR120 (FFAR4) agonist/and a        partial activator of peroxisome proliferator-activated receptors        (PPAR), such as PBI-4547;    -   PRKAA2 gene stimulators/AMPK activators, such as PF-06679142,        PF-06685249;    -   Prostacyclin (PGI2) agonists, such as YS-1402;    -   Protein C activator/Glycoprotein Ib (GPIb) antagonist, such as        AB-002;    -   Protein NOV homolog modulators, such as BLR-200;    -   Protein tyrosine phosphatase-1B inhibitors, such as MSI-1436;    -   Reactive oxygen species modulator inhibitors, such as SUL-121;    -   Renin inhibitors, such as imarikiren hydrochloride;    -   Rho associated protein kinase 2 inhibitors, such as ANG-4201,        RXC-007;    -   Sodium glucose transporter-2 inhibitors, such as canagliflozin,        dapagliflozin propanediol, empagliflozin;    -   Thromboxane A2 receptor antagonist/Thromboxane synthesis        inhibitors, such as SER-150;    -   Tissue transglutaminase inhibitors, such as ZED-1227;    -   TRP cation channel C5 inhibitors, such as GFB-887;    -   TRP cation channel C6 inhibitors, such as ALGX-2224;    -   Cell adhesion molecule inhibitors, such as glycoside bacterial        adhesin antagonists;    -   Urate anion exchanger 1 (URAT1)/SLC22A12 inhibitors, such as        verinurad (RDEA3170);    -   VIP 1/VIP 2 receptor agonists, such as LBT-3627; and    -   Xanthine oxidase inhibitors, such as TMX-049, TMX-049DN.

In some embodiments, the one or more additional therapeutic agents areselected from A-4250, AC-3174, acetylsalicylic acid, AK-20, alipogenetiparvovec, AMX-342, AN-3015, aramchol, ARI-3037MO, ASP-8232, AZD-2693,bertilimumab, Betaine anhydrous, BI-1467335, BMS-986036, BMS-986171,BMT-053011, BOT-191, BTT-1023, CAT-2003, cenicriviroc, CBW-511, CER-209,CF-102, CGS21680, CNX-014, CNX-023, CNX-024, CNX-025, cobiprostone,colesevelam, dapagliflozin, DCR-LIV1, deuterated pioglitazoneR-enantiomer, 2,4-dinitrophenol, DRX-065, DS-102, DUR-928, EDP-305,elafibranor (GFT-505), emricasan, enalapril, ertugliflozin, evogliptin,F-351, fluasterone (ST-002), FT-4101, GKT-831, GNF-5120, GRI-0621,GR-MD-02, GS-300, GS-4997, GS-9674, HTD-1801, HST-202, HST-201,hydrochlorothiazide, icosabutate (PRC-4016), icosapent ethyl ester,IMM-124-E, INT-767, INV-240, IONIS-DGAT2Rx, ipragliflozin, Irbesarta,propagermanium, IVA-337, JKB-121, KB-GE-001, KBP-042, KD-025, M790,M780, M450, metformin, sildenafil, LC-280126, linagliptin, liraglutide,LJN-452 (tropifexor), LM-011, LM-002 (CVI-LM-002), LMB-763, LYN-100,MBX-8025, MDV-4463, mercaptamine, MGL-3196, MGL-3745, MP-301,MSDC-0602K, namacizumab, NC-101, NDI-010976, ND-L02-s0201 (BMS-986263),NGM-282, NGM-313, NGM-386, NGM-395, NP-160, norursodeoxycholic acid,NVP-022, O-304, obeticholic acid (OCA), 25HC3S, olesoxime, PAT-505,PAT-048, PBI-4547, peg-ilodecakin, pioglitazone, pirfenidone, PRI-724,PX20606, Px-102, PX-L603, PX-L493, PXS-4728A, PZ-235, RDX-009,remogliflozin etabonate, RG-125 (AZD4076), RPI-500, saroglitazar,semaglutide, simtuzumab, solithromycin, sotagliflozin, statins(atorvastatin, fluvastatin, pitavastatin, pravastatin, rosuvastatin,simvastatin), symbiotic, TCM-606F, TEV-45478,TQA-3526, tipelukast(MN-001), TLY-012, TRX-318, TVB-2640, UD-009, ursodeoxycholic acid,VBY-376, VBY-825, VK-2809, vismodegib, volixibat potassium ethanolatehydrate (SHP-626), VVP-100X, WAV-301, WNT-974, MU-117, ZGN-839, ZG-5216,ZSYM-008, and ZYSM-007.

In some embodients, the methods and pharmaceutical compositions providedherein include a therapeutically effective amount of an ApoptosisSignal-Regulating Kinase 1 (ASK1) inhibitor and a therapeuticallyeffective amount of an LPAR1 antagonist, wherein the LPAR1 antagonist isa compound of Formula (I), (Ia), (IIa), (IIb), (IIc), (IId), (IIe),(IIf), (IIg), (IIh), or (IIi) provided herein or pharmaceuticallyacceptable salt thereof.

In some embodiments of the methods and pharmaceutical compositionsdisclosed herein, the ASK1 inhibitor is GS-4997 (selonsertib, SEL).

ASK1 inhibitors can be synthesized and characterized using methods knownto those of skill in the art, such as those described in U.S.2007/0276050, U.S. 2011/0009410, and U.S. 2013/0197037.

In some embodients, the methods and pharmaceutical compositions providedherein include a therapeutically effective amount of an Acetyl-CoACarboxylase (ACC) inhibitor and a therapeutically effective amount of anLPAR1 antagonist, wherein the LPAR1 antagonist is a compound of Formula(I), (Ia), (IIa), (IIa), (IIc), (IId), (IIe), (IIf), (IIg), (IIh), or(IIi) provided herein or pharmaceutically acceptable salt thereof.

In some embodiments of the methods and pharmaceutical compositionsdisclosed herein, the ACC inhibitor is GS-0976 (firsocostat, FIR).

ACC inhibitors can be synthesized and characterized using methods knownto those of skill in the art, such as those described in U.S. Pat. Nos.9,453,026 and 10,183,951.

In some embodiments, the methods and compositions provided hereininclude a therapeutically effective amount of a PPAR agonist (e.g., PPARalpha agonist, PPAR alpha/delta agonist, PPARalpha/delta/gamma agonist,PPAR delta agonist) or fish oil, a therapeutically effective amount ofan Acetyl CoA Carboxylase (ACC) inhibitor, such as GS-0976 (firsocostat,FIR), and a therapeutically effective amount of an LPAR1 antagonist,wherein the LPAR1 antagonist is a compound of Formula (I), (Ia), (IIa),(IIb), (IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk),(IIl), (IIm), (IIn), or (IIo), provided herein or pharmaceuticallyacceptable salt thereof. In some embodiments, the PPAR agonist is a PPARalpha agonist. In some embodiments, the PPAR alpha agonist is selectedfrom aluminum clofibrate, bezafibrate, ciprofibrate, cholinefenofibrate, clinofibrate, clofibrate, clofibride, fenofibrate,gemfibrozil, pemafibrate, ronifibrate, simfibrate, pirinixic acid,GW409544, AZ 242, LY518674, NS-220, AVE8134, BMS-711939, aleglitazar,muraglitzar, and saroglitazar. In some embodiments, the PPAR agonist(e.g., PPAR alpha agonist) is a fibrate. In some embodiments, the PPARagonist (e.g., PPAR alpha agonist) is fenofibrate. In some embodiments,the PPAR agonist is a PPAR alpha/delta agonist (e.g., elafibranor). Insome embodiments, the PPAR agonist is a PPAR alpha/delta/gamma agonist(e.g., lanifibranor). In some embodiments, the PPAR agonist is a PPARdelta agonist (e.g., seladelpar). In some embodiments the fish oil is anomega-3 fatty acid or docosahexaenoic acid. In some embodiments, thefish oil is icosapent ethyl (e.g., Vascepa®).

In some embodiments, the methods and compositions provided hereininclude a therapeutically effective amount of a Farnesoid X Receptor(FXR) agonist and a therapeutically effective amount of an LPAR1antagonist, wherein the LPAR1 antagonist is a compound of Formula (I),(Ia), (IIa), (IIb), (IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi),(IIj), (IIk), (IIl), (IIm), (IIn), or (IIo), provided herein orpharmaceutically acceptable salt thereof.

In some embodiments of the methods and pharmaceutical compositionsdisclosed herein, the FXR agonist is GS-9674 (cilofexor, CILO).

In some embodiments of the methods and pharmaceutical compositionsdisclosed herein, the FXR agonist is a compound having the structure:

or a pharmaceutically acceptable salt thereof.

In some embodiments, the methods and compositions provided hereininclude a therapeutically effective amount of a GLP-1 receptor agonistand a therapeutically effective amount of an LPAR1 antagonist, whereinthe LPAR1 antagonist is a compound of Formula (I), (Ia), (II), (IIa),(IIb), (IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk),(IIl), (IIm), (IIn), or (IIo) provided herein or a pharmaceuticallyacceptable salt thereof. In some embodiments, the GLP-1 receptor agonistis liraglutide or semaglutide. In some embodiments, the GLP-1 receptoragonist is semaglutide.

In some embodiments, the methods and compositions provided hereininclude a therapeutically effective amount of a TGFβ antagonist and atherapeutically effective amount of an LPAR1 antagonist, wherein theLPAR1 antagonist is a compound of Formula (I), (Ia), (IIa), (IIb),(IIc), (IId), (IIe), (IIf), (IIg), (IIh), (IIi), (IIj), (IIk), (IIl),(IIm), (IIn), or (IIo), provided herein or pharmaceutically acceptablesalt thereof. In some embodiments, the TGFβ antagonist is aTGFβ-specific antibody. TGFβ-specific antibodies can be prepared andcharacterized using methods known to those of skill in the art, such asthose described in PCT International Application Publication No. WO2018/129329 and in U.S. Pat. No. 9,518,112. In some embodiments, theTGFβ antagonist binds to a TGFβ latency-associated peptide (LAP), e.g.,TGFβ 1-LAP. TGFβ 1-LAP-specific antibodies can be prepared andcharacterized using methods known to those of skill in the art, such asthose described in U.S. Pat. No. 8,198,412 or U.S. Pat. No. 10,017,567.In some embodiments, the TGFβ antagonist binds to TGFβ (e.g., TGFβ 1) ina context independent manner (e.g., independent of the presentation ofTGFβ in a specific tissue or organ). In some embodiments, the TGFβantagonist binds to TGFβ (e.g., TGFβ 1) in a context-dependent manner.In some embodiments, the TGFβ antagonist blocks activation of latentTGFβ (e.g., latent TGFβ 1) that is localized in extracellular matrix,e.g., in connective tissue of the liver. In some embodiments, the TGFβantagonist blocks activation of latent TGFβ (e.g., latent TGFβ 1) thatis localized in the thymus, a lymph node, or in a tumor microenvironment(e.g., in a patient having liver cancer). In some embodiments, the TGFβantagonist blocks activation of latent TGFβ (e.g., latent TGFβ 1) byLatent TGFβ Binding Protein (LTBP). In some embodiments, the TGFβantagonist blocks activation of latent TGFβ (e.g., latent TGFβ 1) byGlycoprotein-A Repetitions Predominant protein (GARP), as described,e.g., in U.S. Pat. No. 10,000,572. In some embodiments, the TGFβantagonist is ARGX-115. In some embodiments, the TGFβ antagonist is ananti-latency-associated peptide (LAP) antibody that specifically bindsto a LAP-TGFβ complex. In some embodiments, the anti-LAP antibodyspecifically binds to LAP-TGFβ complexes in extracellular matrix (ECM),e.g., of connective tissue in the liver. In some embodiments, theanti-LAP antibody specifically binds to LAP-TGFβ complexes on thesurfaces of certain immunosuppressive cell types, such as regulatory Tcells (Tregs), tumor-associated macrophages, or myeloid-derivedsuppressor cells, e.g., in a tumor microenvironment. In someembodiments, the anti-LAP antibody is a TLS-01 antibody. In someembodiments, the anti-LAP antibody specifically binds to LAP-TGFβcomplexes in any context. In some embodiments, the anti-LAP antibody isa TLS-02 antibody. In some embodiments, the TGFβ antagonist comprises aTGFβ receptor. In some embodiments, the TGFβ antagonist is a TGFβreceptor-Fc fusion protein. In some embodiments, the TGFβ antagonist isan antibody comprising a TGFβ receptor. TGFβ antagonists comprising aTGFβ receptor that can be useful in connection with the compositions andmethods provided herein have been described, e.g., in PCT InternationalPublication Nos. WO 2019/113123 A1 and WO 2019/113464 A1.

In some embodiments the methods and compositions provided herein includea therapeutically effective amount of an LPAR1 antagonist and of anadditional therapeutic agent selected from an ACE inhibitor, adenosineA3 receptor antagonist, adropin stimulator, albumin modulator,aldosterone antagonist, AMP activated protein kinase stimulator,angiotensin II AT-2 receptor agonist, angiotensin II receptorantagonist, angiotensinogen ligand inhibitor, APOA1 gene stimulator,apolipoprotein L1 modulator, bone morphogenetic protein-7 ligandmodulator, bromodomain containing protein 2 inhibitor, bromodomaincontaining protein 4 inhibitor, calcium channel inhibitors, cannabinoidCB1 receptor antagonists, CB1 inverse agonists, CCR2 chemokineantagonist, chymase inhibitor, complement C1s subcomponent inhibitor,CX3CR1 chemokine antagonist, cyclooxygenase 1 inhibitor, cyclooxygenase2 inhibitor, cytochrome P450 11B2 inhibitor, ectonucleotidepyrophosphatase-PDE-2 inhibitor, endothelin ET-A receptor antagonist,endothelin ET-B receptor antagonist, enteropeptidase inhibitor, epoxidehydrolase inhibitor, erythropoietin receptor antagonist, farnesoid Xreceptor agonist, FGF receptor antagonists, free fatty acid receptor 1agonist, GHR gene inhibitor, glycoprotein Ib (GPIb) antagonist, GPR40agonist, GPR84 antagonist, G-protein beta subunit inhibitor, G-proteincoupled receptor 120 agonist, G-protein coupled receptor 84 modulator,growth hormone ligand, growth hormone receptor agonist, guanylatecyclase receptor agonists, guanylate cyclase stimulator, heme oxygenase1 modulator, HIF prolyl hydroxylase inhibitor, IGF1 gene inhibitors, IgGreceptor FcRn large subunit p51 modulator, IL-6 receptor antagonist,integrin alpha-V/beta-3 antagonist, interleukin 33 ligand inhibitor,Kelch-like ECH associated protein 1 modulator, LDHA gene inhibitor,5-lipoxygenase activating protein inhibitor, lysophosphatidate-1receptor antagonist, matrix extracellular phosphoglycoprotein modulator,membrane copper amine oxidase inhibitor, midkine ligand inhibitor,mineralocorticoid receptor antagonist, myosin 2 inhibitors, NADPHoxidase 1 inhibitor, NADPH oxidase 4 inhibitor, NADPH oxidase inhibitor,NK1 receptor antagonist, nuclear erythroid 2-related factor 2stimulator, nuclear factor kappa B inhibitor, opioid receptor kappaagonist, opioid receptor mu antagonists p38 MAP kinase inhibitor, PDE4inhibitor, PDGF receptor antagonist, PDGF receptor beta modulator,phosphatonin receptor agonist, PRKAA2 gene stimulator, proproteinconvertase PC9 inhibitor, prostacyclin (PGI2) agonist, protein Cactivator, protein NOV homolog modulator, protein tyrosinephosphatase-1B inhibitor, reactive oxygen species modulator inhibitor,renin inhibitor, Rho associated protein kinase 2 inhibitor, SLC22A12inhibitor, sodium glucose transporter-2 inhibitor, solute carrier familyinhibitor, TGF beta ligand inhibitor, TGF beta receptor antagonist,thromboxane A2 receptor antagonist, thromboxane synthesis inhibitor,tissue transglutaminase inhibitor, TRP cation channel C5 inhibitor, TRPcation channel C6 inhibitor, tryptophanase inhibitor, unspecified celladhesion molecule inhibitor, urate anion exchanger 1 inhibitor,vasopressin V1a receptor antagonist, VEGF receptor antagonist, VIP 1receptor agonist, VIP 2 receptor agonist, and Xanthine oxidaseinhibitor.

In some embodiments the methods and compositions provided herein includea therapeutically effective amount of an LPAR1 antagonist and of anadditional therapeutic agent selected from a VEGFR inhibitor, a FGFRinhibitor, a PDGFR inhibitor, an autaxin inhibitor, a GPR84 agonist, aPASK inhibitor, a CFTR agonist, a JAK1 inhibitor, an ADAMTS5 inhibitor,a TOL2/3 inhibitor, a CTGF inhibitor, a soluble PTX2, an anti-galectin-3antibody, an integrin-α_(V)-β₆/α_(V)-β₁ antagonist, a JNK1 inhibitor, amineralocorticoid receptor antagonist, a Nrf2 activator, a chymaseinhibitor, a PDE inhibitor, a NOX1/4 inhibitor, aleukotriene/thromboxane receptor antagonist, SLC22A12 inhibitor, an sGCinhibitor, and a xanthine oxidase inhibitor.

In some embodiments the methods and compositions provided herein includea therapeutically effective amount of an LPAR1 antagonist and of anadditional therapeutic agent selected from nintedanib, pirfenidone,pamrevlumab, PRM-151, GB-0139, PLN-74809, CC-90001, finerenone,BAY1142524, PCS-499, setanaxib, SER150, RDEA3170, praliciguat, TMX-049,GLPG1690, GLPG1205, GLPG1972, GLPG4059, GLPG2737, GLPG3970, andfilgotinib.

In some embodiments the methods and compositions provided herein includea therapeutically effective amount of an LPAR1 antagonist and of anadditional therapeutic agent selected from A-717, ACF-TEI,alanyl-glutamine, ALLN-346, anti-SCF248 antibody, anti-TAGE monoclonalantibodies, anti-TGF beta antibodies, AST-120, BAY-2327949, BI-685509,DP-001, DZ-4001, GDT-01, LNP-1892, MEDI-8367, microRNA-targetingantisense oligonucleotide therapy, MK-2060, MPC-300-IV, NAV-003,Neo-Kidney Augment™ (NKA), NP-135, NP-160, NP-251, NRF-803, PBI-4610,PHN-033, R-HSC-010, salvianolic acid, SGF-3, SPD-01, Sugaheal variant,SZ-005, TCF-12, ITMC119-06, VAR-400, veverimer, VS-105, and XRx-221.

EXAMPLES

The following examples are included to demonstrate specific embodimentsof the disclosure. It should be appreciated by those of skill in the artthat the techniques disclosed in the examples which follow representtechniques to function well in the practice of the disclosure, and thuscan be considered to constitute specific modes for its practice.However, those of skill in the art should, in light of the presentdisclosure, appreciate that these examples are exemplary and notexhaustive. Many changes can be made in the specific embodiments whichare disclosed and still obtain a like or similar result withoutdeparting from the spirit and scope of the disclosure.

Compounds disclosed herein can be prepared according to the proceduresof the following Schemes and Examples, using appropriate materials andare further exemplified by the following specific examples. Moreover, byutilizing the procedures described herein, in conjunction with ordinaryskills in the art, additional compounds of the present disclosureclaimed herein can be readily prepared. The examples further illustratedetails for the preparation of the compounds of the present disclosure.Those skilled in the art will readily understand that known variationsof the conditions and processes of the following preparative procedurescan be used to prepare these compounds. For synthesizing compounds whichare embodiments described in the present disclosure, inspection of thestructure of the compound to be synthesized will provide the identity ofeach substituent group. In some cases, the identity of the final productcan render apparent the identity of the necessary starting materials bya process of inspection, given the examples herein. Compounds can beisolated in the form of their pharmaceutically acceptable salts, such asthose described above. Compounds described herein are typically stableand isolatable at room temperature and pressure.

An illustration of the preparation of compounds disclosed herein isshown below. Unless otherwise indicated, variables have the same meaningas described above. The examples presented below are intended toillustrate particular embodiments of the disclosure. Suitable startingmaterials, building blocks and reagents employed in the synthesis asdescribed below are commercially available from AbovChem, AcrosOrganics, Astatech, Combi Blocks, Oakwood Chemical, or Sigma-Aldrich,for example, or can be routinely prepared by procedures described in theliterature, for example in “March's Advanced Organic Chemistry:Reactions, Mechanisms, and Structure”, 5^(th) Edition; John Wiley & Sonsor T. Eicher, S. Hauptmann “The Chemistry of Heterocycles; Structures,Reactions, Synthesis and Application”, 2^(nd) edition, Wiley-VCH 2003;Fieser et al. “Fiesers' Reagents for organic Synthesis” John Wiley &Sons 2000.

General Schemes

Scheme A provides a general synthesis of triazole carbamate aryl- andheteroaryl-carboxamides (VI). In the Schemes disclosed herein “A” can bea halogen such as Cl, Br, or I. Aryl or heteroaryl halide (I) can bereadily prepared by electrophilic aromatic halogenation of thecorresponding aryl or heteroaryl amine. Step one describes the acylationof aryl and heteroaryl amines (I). Amine (I) can be treated with an acidchloride, or a carboxylic acid with standard peptide coupling conditionssuch as the use of 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC)to provide the corresponding amides (II). Alternatively, the amine (I)can also be treated with a chloroformate, to provide the correspondingcarbamate (II). Additionally, the amine (I) can be treated first withphosgene, to generate the intermediate isocyanate, which can then betrapped by an amine to provide the corresponding urea (II).

Step two describes a general synthesis of aryl or heteroaryl triazolecarboxylic acids (IV) via cross coupling reaction. Aryl or heteroarylhalide (II) can first be converted to the corresponding boronic estersuch as pinacol boronate via Miyaura borylation, and then subjected toSuzuki reaction conditions with bromo triazole carboxylic acid (III) tofurnish the desired aryl or heteroaryl triazole carboxylic acid (IV).Alternatively, bromo triazole carboxylic acid (III) can first beconverted to an organo-zinc species via lithium-halogen exchange andtrapping with zinc chloride. Next, Negishi cross coupling with aryl orheteroaryl halide (II) provides the desired aryl or heteroaryl triazolecarboxylic acid (IV).

Step three describes a general synthesis of triazole carbamate aryl- andheteroaryl-carboxamides (VI). An aryl or heteroaryl triazole carboxylicacid (IV) undergoes a Curtius rearrangement when treated withdiphenylphosphoryl azide (DPPA), or alternatively with1-propanephosphonic anhydride (T3P) solution and azidotrimethylsilane.The intermediate isocyanate is then trapped with an alcohol (V) toprovide the desired aryl or heteroaryl triazole carbamate (VI).

Scheme B provides an alternative synthesis of triazole carbamate aryl-and heteroaryl-carboxamides (VI). Step one describes a general synthesisof amino-aryl or -heteroaryl triazole carbamates (XI) via cross couplingreaction. Bromo triazole carbamate (X) can first be converted to anorgano-zinc species via lithium-halogen exchange and trapping with zincchloride. Next, Negishi cross coupling with aryl or heteroaryl halide(I), provides the desired amino-aryl or -heteroaryl triazole carbamate(XI). Alternatively, aryl or heteroaryl halide (I) can first beconverted to the corresponding boronic ester such as pinacol boronatevia Miyaura borylation, and then subjected to Suzuki reaction conditionswith bromo triazole carbamate (X) to furnish the desired amino-aryl or-heteroaryl triazole carbamate (XI).

Step 1A-B describes an alternative synthesis to amino-aryl or-heteroaryl triazole carbamate (XI). Tert-butyl carbamate (XII) can bereadily prepared by treatment of the corresponding aryl or heteroarylamines with di-tert-butyl dicarbonate. Aryl or heteroaryl halide (XII)can first be converted to the corresponding boronic ester such aspinacol boronate via Miyaura borylation, and then subjected to Suzukireaction conditions with bromo triazole carbamate (X) to furnish thedesired aryl or heteroaryl triazole carbamate (XIII). Alternatively,bromo triazole carbamate (X) can first be converted to an organo-zincspecies via lithium-halogen exchange and trapping with zinc chloride.Next, Negishi cross coupling with aryl or heteroaryl halide (XII)provides the desired aryl or heteroaryl triazole carbamate (XIII). Next,the tert-butyl aryl or heteroaryl triazole carbamate (XIII) can betreated with acids such as hydrogen chloride (HCl) to furnish theamino-aryl or -heteroaryl triazole carbamate (XI) as the hydrochloridesalt.

Step two describes the general synthesis of triazole carbamate aryl- andheteroaryl-carboxamides (VI). The amino-aryl or -heteroaryl triazolecarbamate (XI) can be treated with an acid chloride, or a carboxylicacid with standard peptide coupling conditions such as the use of1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) to provide thecorresponding amides (VI). Alternatively, the amine (XI) can also betreated with a chloroformate, to provide the corresponding carbamate(VI). Additionally, the amine (XI) can be treated first with phosgene,to generate the intermediate isocyanate, which can then be trapped by anamine to provide the corresponding urea (VI).

Scheme C provides a general alternative synthesis of aryl or heteroaryltriazole carbamates (VI). Step one describes a general synthesis of arylor heteroaryl triazole carboxylic acids (XIV) via cross couplingreaction. Aryl or heteroaryl halide (XII) can first be converted to thecorresponding boronic ester such as pinacol boronate via Miyauraborylation, and then subjected to Suzuki reaction conditions with bromotriazole carboxylic acid (III) to furnish the desired aryl or heteroaryltriazole carboxylic acid (XIV). Alternatively, bromo triazole carboxylicacid (III) can first be converted to an organo-zinc species vialithium-halogen exchange and trapping with zinc chloride. Next, Negishicross coupling with aryl or heteroaryl halide (XII) provides the desiredaryl or heteroaryl triazole carboxylic acid (XIV).

Step two describes a general synthesis of carbamate containing aryl orheteroaryl triazoles (XIII) An aryl or heteroaryl triazole carboxylicacid (XIV) undergoes a Curtius rearrangement when treated withdiphenylphosphoryl azide (DPPA), or alternatively with1-propanephosphonic anhydride (T3P) solution and azidotrimethylsilane.The intermediate isocyanate is then trapped with an alcohol (V) toprovide the desired aryl or heteroaryl triazole carbamate (XIII) Stepthree describes a general synthesis of amino-aryl or -heteroaryltriazole carbamate (XI). Tert-butyl aryl or heteroaryl carbamate (XIII)can be treated with acids such as hydrogen chloride (HCl) to furnish theamino-aryl or -heteroaryl triazole carbamate (XI) as the hydrochloridesalt.

Step four describes the general synthesis of triazole carbamate aryl-and heteroaryl-carboxamides (VI). The amino-aryl or -heteroaryl triazolecarbamate (XI) can be treated with an acid chloride, or a carboxylicacid with standard peptide coupling conditions such as the use of1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) to provide thecorresponding amides (VI). Alternatively, the amine (XI) can also betreated with a chloroformate, to provide the corresponding carbamate(VI). In the case where phenyl chloroformate is used, the resultingphenyl carbamate (VI) can be treated with an amine to generate thecorresponding urea (VI). Additionally, the amine (XI) can be treatedfirst with phosgene, to generate the intermediate isocyanate, which canthen be trapped by an amine to provide the corresponding urea (VI).

Scheme D describes an alternative synthesis of synthesis of triazolecarbamate aryl- and heteroaryl-carboxamides (VI). E can be a halogen,such as —Br or —I. In step one, an aryl- or heteroaryl-dihalide (XV)undergoes a Sonagashira coupling with propargyl alcohol to generate thearyl- or heteroaryl-alkyne (XVI). The alkyne then ungoes a thermal orcatalytic cycloaddition with an azide to generate the correspondinghydroxymethyl triazoles (XVII) in step two. Finally, oxidation of theprimary alcohol using tetramethylpiperidinyloxy (TEMPO), and sodiumchlorite provides the triazole carboxylic acid (XVIII) in step three.

In step four, the triazole carboxylic acid (XVIII) is protected as amethyl ester (XIX) such as by treatment with thionyl chloride. In stepfive, the aryl- or heteroaryl-halide (XIX) then undergoes aBuchwald-type amination with tert-butyl carbamate to generate theBoc-protected amine (XX).

In step six, exposure of Boc-protected amine (XX) to hydrochloric acidreveals the hydrochloride salt (XXI), which can be reacted in step sevenwith an acid chloride, or a carboxylic acid with standard peptidecoupling conditions such as the use of1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) to provide thecorresponding amides (XXII). Alternatively, the amine (XXI) can also betreated with a chloroformate, to provide the corresponding carbamate(XXII). Additionally, the amine (XXI) can be treated first withphosgene, to generate the intermediate isocyanate, which can then betrapped by an amine to provide the corresponding urea (XXII). In stepeight, the triazole ester (XXII) can be hydrolyzed upon treatment withbase such as sodium hydroxide, to reveal the triazole carboxylic acid(IV). Lastly, step nine describes a Curtius rearrangement of triazolecarboxylic acids (IV) via treatment with diphenylphosphoryl azide(DPPA), or alternatively with 1-propanephosphonic anhydride (T3P)solution and azidotrimethylsilane. The intermediate isocyanate is thentrapped with an alcohol (V) to provide the desired aryl- orheteroaryl-triazole carbamate (VI).

Example 1 Preparation of 4-bromo-1-methyl-1H-1,2,3-triazole-5-carboxylicacid (Intermediate 1)

Step 1: 4,5-dibromo-2H-1,2,3-triazole

Bromine (2.8 mol) was added to a solution of 2H-1,2,3-triazole (1.4 mol)in water (600 mL) at 40° C. The resulting mixture was stirred for 2hours at 40° C. After cooling to room temperature, the precipitate wascollected by filtration. The solid was washed with water (2×300 mL) anddried under vacuum to give 4,5-dibromo-2H-1,2,3-triazole.

Step 2: 4,5-dibromo-1-methyl-1H-1,2,3-triazole

To a mixture of 4,5-dibromo-2H-1,2,3-triazole (704 mmol) and K₂CO₃ (1.4mol) in THF (1000 mL), iodomethane (1.0 mol) was added. The mixture wasstirred for 12 hours at room temperature. The mixture was filtered, andthe filter cake was washed with ethyl acetate (2×500 mL), the filtratewas concentrated under 40° C. to afford a crude product, which waspurified by column chromatography to give4,5-dibromo-1-methyl-1H-1,2,3-triazole.

Step 3: 4-bromo-1-methyl-1H-1,2,3-triazole-5-carbaldehyde

To a solution of 4,5-dibromo-1-methyl-1H-1,2,3-triazole (168.0 mmol) inTHF (600 mL) was added isopropylmagnesium chloride (252.0 mmol) at −10°C. The mixture was stirred for 15 min, DMF (840 mmol) was added. After 1hour, the mixture was treated with 250 mL of saturated ammonium chlorideand extracted with DCM (2×350 mL). The combined organics were washedwith 250 mL of brine, dried over Na₂SO₄, filtered and concentrated togive 4-bromo-1-methyl-1H-1,2,3-triazole-5-carbaldehyde.

Step 4: 4-bromo-1-methyl-1H-1,2,3-triazole-5-carboxylic acid

Oxone (651 mmol) was added to a solution of4-bromo-1-methyl-1H-1,2,3-triazole-5-carbaldehyde (536 mmol) in DMF (800mL) and the resulting suspension was stirred at room temperatureovernight. The mixture reaction was diluted with H₂O (1000 mL), wasadjusted to pH 3 with 1N HCl, and the aqueous phase was extracted withethyl acetate (3×800 mL). The combined organics were washed withsaturated Na₂CO₃ (2×500 mL), the aqueous phase was adjusted to pH 3 with1N HCl. The precipitate was isolated by filtration and dried underreduced pressure to provide4-bromo-1-methyl-1H-1,2,3-triazole-5-carboxylic acid (Intermediate 1).

Example 2 Preparation of (R)-1-(2-chlorophenyl)ethyl(4-bromo-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (Intermediate 2A)

To a suspension of 4-bromo-1-methyl-1H-1,2,3-triazole-5-carboxylic acid(24.3 mmol) in toluene (80 mL) was added DPPA (24.5 mmol), triethylamine(24.5 mmol), and (R)-1-(2-chlorophenyl)ethan-1-ol (36.5 mmol). Themixture was heated at 80° C. for 3 hours. The reaction mixture wasfiltered, and the filtrate was concentrated in vacuo. The residue waspurified by silica chromatography to afford (R)-1-(2-chlorophenyl)ethyl(4-bromo-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (Intermediate 2A).

Example 3 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(4-bromo-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (Intermediate 2B)

4-Bromo-1-methyl-1H-1,2,3-triazole-5-carboxylic acid (95 mmol), 50%1-propanephosphonic anhydride solution (143 mmol) in DMF, andazidotrimethylsilane (143 mmol), were suspended in THF (350 mL) under anatmosphere of argon. Triethylamine (143 mmol) was added and theresulting solution was allowed to stir for 30 minutes.(R)-1-(2-chloropyridin-3-yl)ethan-1-ol (143 mmol) was added and themixture was heated at reflux, with a secondary bubbler attached to allowfor venting, for 12 hours. The reaction mixture was cooled to roomtemperature, and the THF was removed in vacuo. The resulting crudematerial was dissolved in 500 mL ethyl acetate and extracted three timeswith 300 mL water. The crude mixture was then dried over sodium sulfate,filtered and the filtrate was concentrated. The crude was purified bysilica gel column chromatography to provide(R)-1-(2-chloropyridin-3-yl)ethyl(4-bromo-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (Intermediate 2B).

Example 4 Preparation of (R)-1-(2-fluoropyridin-3-yl)ethyl(4-bromo-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (Intermediate 2C)

Following the procedure described in Example 3 for the synthesis of(R)-1-(2-chloropyridin-3-yl)ethyl(4-bromo-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (Intermediate 2B),using (R)-1-(2-fluoropyridin-3-yl)ethan-1-ol (143 mmol) in place of(R)-1-(2-chloropyridin-3-yl)ethan-1-ol,(R)-1-(2-fluoropyridin-3-yl)ethyl(4-bromo-1-methyl-1H-1,2,3-triazol-5-yl)carbamate was obtained(Intermediate 2C).

Example 5 Preparation of (R)-1-(3-fluorophenyl)ethyl(4-bromo-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (Intermediate 2D)

Following the procedure described in Example 3 for the synthesis of(R)-1-(2-chloropyridin-3-yl)ethyl(4-bromo-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (Intermediate 2B),using (R)-1-(3-fluorophenyl) ethan-1-ol (230 mmol) in place of(R)-1-(2-chloropyridin-3-yl)ethan-1-ol, (R)-1-(3-fluorophenyl)ethyl(4-bromo-1-methyl-1H-1,2,3-triazol-5-yl)carbamate was obtained(Intermediate 2D).

Example 6 Preparation of methyl4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylate(Intermediate 3A)

Intermediate 3A was generally prepared according to Scheme D.

Step 1: 3-(5-bromopyridin-2-yl)prop-2-yn-1-ol

To a mixture of 5-bromo-2-iodopyridine (352.2 mmol) in THF (400 mL) wasadded Compound prop-2-yn-1-ol (370 mmol), triethylamine (1.06 mol),cuprous iodide (17.6 mmol) and bis(triphenylphosphine) palladium(II)chloride (10.6 mmol) under nitrogen atmosphere. The reaction mixture wasstirred at room temperature for 16 hours. After completion of thereaction, the mixture was diluted with water (500 ml) and the solid wasfiltered. The filtrate was extracted with ethyl acetate (3×500 ml). Theorganic layer was dried over anhydrous sodium sulfate and concentratedunder reduced pressure. The residue was triturated with ethyl acetateand ether and stirred for 2 hours and filtered. The filter cake waswashed with ether to give 3-(5-bromopyridin-2-yl)prop-2-yn-1-ol.

Step 2: (4-(5-bromopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)methanol

Cuprous iodide (0.94 mmol) and tetrabutylammonium iodide (0.94 mmol)were mixed together and dissolved in THF (30 mL), stirred for 20 minutesto yield a solution. Then, 3-(5-bromo-2-pyridyl)prop-2-yn-1-ol (9.43mmol) was added and the reaction was sparged with argon for 2 minutes.Pentamethylcyclopentadienylbis(triphenylphosphine)ruthenium(II) chloride(0.47 mmol) and azidomethyltrimethylsilane (24 mmol) were added and thereaction was sealed and heated to 80° C. for 16 hours. The reactionmixture was concentrated in vacuo, and then re-dissolved in THF (50 mL).Tetrabutylammonium fluoride (10 mL of a 1 M solution in THF) was addeddropwise at room temperature and stirred for 1 hour. The mixture wasquenched with saturated solution of sodium bicarbonate (100 mL) andextracted with DCM (3×100 mL). The organic layer was dried overanhydrous sodium sulfate and concentrated under reduced pressure. Theresidue was purified by silica gel chromatography to provide(4-(5-bromopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)methanol.

Step 3: 4-(5-bromopyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid

[5-(5-bromo-2-pyridyl)-3-methyl-triazol-4-yl]methanol (4.83 mmol),2,2,6,6-tetramethylpiperidinyloxy (TEMPO) (0.48 mmol), and sodiumphosphate monobasic (12.08 mmol) were suspended in acetonitrile (50 ml)and water (40 ml). The solution was heated to 45° C. Then, 10 ml of a 1M aqueous solution of sodium chlorite and a separate solution of sodiumhypochlorite (10 ml of 0.01 M solution in water), were addedsimultaneously over 1 hour. The reaction was stirred at 45° C. for 16hours. The mixture was cooled to room temperature and concentrated toremove acetonitrile. The product was filtered and the filter cake waswashed with water (2×50 mL), and diethyl ether (50 mL) to provide4-(5-bromopyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylic acid.LCMS M/Z (M+1)=283.1.

Step 4: methyl4-(5-bromopyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylate

4-(5-bromopyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylic acid(14.1 mmol) was dissolved in 40 ml of methanol. The solution was cooledto 0° C. with an ice bath. Trimethylsilyldiazomethane (18.4 mmol) wasadded dropwise over 15 min. The ice bath was removed and the reactionwas stirred for 5 hours. The reaction was quenched by the addition ofsaturated aqueous sodium bicarbonate and extracted with ethyl acetate.The organic layer was dried over anhydrous sodium sulfate andconcentrated under reduced pressure. The residue was purified by silicagel chromatography to provide methyl4-(5-bromopyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylate.

Step 5: Methyl4-(5-((tert-butoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylate

Methyl 4-(5-bromopyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylate(11.1 mmol), tert-butyl carbamate (33 mmol), cesium carbonate (33 mmol),and Xantphos Pd G3 pre-catalyst (1.1 mmol) were suspended in dioxane (50ml). The suspension was sparged with argon for 10 minutes and thenheated to 95° C. for 4 hours. After completion of the reaction, themixture was cooled and diluted with water (100 ml) and extracted withethyl acetate (2×100 ml). The organic layer was dried over anhydroussodium sulfate and concentrated under reduced pressure. The residue waspurified by silica gel chromatography to provide methyl4-(5-((tert-butoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylate.

Step 6: Methyl4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylatehydrochloride salt (Intermediate 3A)

To methyl4-(5-((tert-butoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylate(6 mmol), was added 4M HCl in dioxanes (14 mL) and the reaction wasstirred vigorously at room temperature for 3 hours. After completion ofthe reaction, the solution was concentrated in vacuo to provide methyl4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylatehydrochloride salt (Intermediate 3A).

Example 7 Preparation of4-(5-((tert-butoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid (Intermediate 3B)

4-bromo-1-methyl-1H-1,2,3-triazole-5-carboxylic acid (50 mmol) wasdissolved in 500 mL of tetrahydrofuran and submerged in a −78° C. bathfor 15 minutes. A 1 M solution of Lithium bis(trimethylsilyl)amide intetrahydrofuran (54 mmol) was dropwise over 15 minutes. A 2.5 M solutionof n-butylithium (105 mmol) in hexanes was added dropwise over 20minutes and allowed to stir for an additional 1 hour. A 1.9 M solutionof zinc chloride (105 mmol) in 2-methyl tetrahydrofuran was addeddropwise over 15 minutes. The reaction mixture was warmed to ambienttemperature by submerging in a water bath and allowed to stir for 30minutes. The resulting mixture was sparged with argon gas for 10 min,and then tert-butyl (6-bromopyridin-3-yl)carbamate (50 mmol) and[1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II), complexwith dichloromethane (5 mmol) were added. The reaction was heated at 75°C. for 3 hours, and then cooled to ambient temperature. The reaction wasdiluted with 350 mL of a 2 M aqueous solution of sodium hydroxide and300 mL of diethyl ether. The aqueous layer was separated, and theorganic layer was extract with a 1 M aqueous solution of sodiumhydroxide (100 mL). The combined aqueous layer was washed with a 1:1mixture of ethyl acetate and diethyl ether (150 mL×2). 80 mL ofconcentrated hydrochloric acid was dropwise over 10 min under vigorousstirring to adjust pH to 4. The mixture was filtered, and the filtercake was washed with water (100 mL) and a 1:1 mixture of ethyl acetateand diethyl ether (100 mL×2). The precipitate was dried under reducedpressure to provide4-(5-((tert-butoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid (Intermediate 3B).

Example 8 Preparation of (R)-1-(3-fluorophenyl)ethyl(1-methyl-4-(4-(2,2,2-trifluoroacetamido)phenyl)-1H-1,2,3-triazol-5-yl)carbamate(Compound 1)

Step 1: (R)-1-(3-fluorophenyl)ethyl(4-(4-aminophenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

A mixture of (R)-1-(3-fluorophenyl)ethyl(4-bromo-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (Intermediate 2D)(0.370 mmol), 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline(0.407 mmol), tetrakis(triphenylphosphine)palladium(0) (0.037 mmol) andsodium carbonate (1.11 mmol) in 1,4-dioxane/water (3:1, 3.0 mL) wasdegassed with argon for 10 minutes. The vessel was sealed and heated at100° C. for 18 hours. The reaction was cooled to room temperature,diluted with saturated aqueous NH₄Cl and extracted with dichloromethane.The combined organic layers were washed with brine, dried over MgSO₄,filtered and concentrated under reduced pressure. The crude material waspurified by silica gel chromatography to provide(R)-1-(3-fluorophenyl)ethyl(4-(4-aminophenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 8C).

Step 2: (R)-1-(3-fluorophenyl)ethyl(1-methyl-4-(4-(2,2,2-trifluoroacetamido)phenyl)-1H-1,2,3-triazol-5-yl)carbamate(Compound 1)

To a solution of (R)-1-(3-fluorophenyl)ethyl(4-(4-aminophenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 8C) (0.082 mmol) in dichloromethane (2.0 mL) was addedtrifluoroacetic anhydride (0.122 mmol). The solution was stirred at roomtemperature for 3 hours. The reaction was concentrated under reducedpressure and purified by reverse phase chromatography to provide(R)-1-(3-fluorophenyl)ethyl(1-methyl-4-(4-(2,2,2-trifluoroacetamido)phenyl)-1H-1,2,3-triazol-5-yl)carbamate(Compound 6). (MS (m/z) 452.0 [M+H]⁺). 1H NMR (400 MHz, DMSO-d6, mixtureof rotamers) δ 11.36 (s, 1H), 9.97 (major) and 9.55 (minor) (s, 1H),7.73 (s, 4H), 7.53-6.66 (m, 4H), 5.89-5.60 (m, 1H), 3.85 (s, 3H), 1.56(major) and 1.24 (minor) (s, 3H).

Example 9 Preparation of [(1R)-1-(2-chloro-3-pyridyl)ethyl]N-[5-[5-[(1-cyanocyclopropanecarbonyl)amino]pyrimidin-2-yl]-3-methyl-triazol-4-yl]carbamate(Compound 2)

Step 1: [(1R)-1-(2-chloro-3-pyridyl)ethyl]N-[5-(5-aminopyrimidin-2-yl)-3-methyl-triazol-4-yl]carbamate

To a mixture of (R)-1-(2-chloropyridin-3-yl)ethyl(4-bromo-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (Intermediate 2B)(1.39 mmol) in tetrahydrofuran (14 mL) at −78° C. was added a 1 Msolution of lithium bis(trimethylsilyl)amide (1.53 mmol) in THF. After10 minutes, a 2.5 M solution of n-butyllithium (2.77 mmol) in hexaneswas added. After 45 minutes, a 1.9 M solution of zinc chloride (4.30mmol) in 2-MeTHF was added, and the reaction was stirred at roomtemperature for 45 minutes. At this point 2-bromopyrimidin-5-amine (1.94mmol) and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II),complex with dichloromethane (0.139 mmol) were added to the reaction andthe reaction mixture was heated to 70° C. for 1 hour. After completionof the reaction, the mixture was cooled and quenched with saturatedaqueous ammonium chloride. The mixture was diluted with ethyl acetateand organics were separated. The aqueous layer was extracted with ethylacetate (3×10 mL). The combined organic layers were dried over anhydroussodium sulfate and concentrated under reduced pressure. The residue waspurified by column chromatography to provide[(1R)-1-(2-chloro-3-pyridyl)ethyl]N-[5-(5-aminopyrimidin-2-yl)-3-methyl-triazol-4-yl]carbamate.

Step 2:[(1R)-1-(2-chloro-3-pyridyl)ethyl]N-[5-[5-[(1-cyanocyclopropanecarbonyl)amino]pyrimidin-2-yl]-3-methyl-triazol-4-yl]carbamate(Compound 2)

A mixture of [(1R)-1-(2-chloro-3-pyridyl)ethyl]N-[5-(5-aminopyrimidin-2-yl)-3-methyl-triazol-4-yl]carbamate (0.08mmol), 1-cyanocyclopropanecarboxylic acid (0.096 mmol), and1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.096 mmol)in pyridine (1.0 mL) was stirred at room temperature for 30 minutes.After completion of the reaction, the mixture was concentrated underreduced pressure. The residue was purified by reverse-phase HPLC toprovide [(1R)-1-(2-chloro-3-pyridyl)ethyl]N-[5-[5-[(1-cyanocyclopropanecarbonyl)amino]pyrimidin-2-yl]-3-methyl-triazol-4-yl]carbamate.(MS (m/z) 468.1 [M+H]⁺). ¹H NMR (400 MHz, Methanol-d₄) δ 9.04 (s, 2H),8.30 (s, 1H), 8.00 (s, 1H), 7.45 (s, 1H), 6.08 (q, J=6.7 Hz, 1H), 3.99(s, 3H), 1.82-1.75 (m, 2H), 1.73-1.67 (m, 2H), 1.59 (s, 3H).

Example 10 Preparation of Compounds 3 and 4

Compounds 3 and 4 were generally synthesized according Scheme B, Step 1.For example, (R)-1-(2-chloropyridin-3-yl)ethyl(1-methyl-4-(6-(3-methylureido)pyridin-3-yl)-1H-1,2,3-triazol-5-yl)carbamate(Compound 3) was prepared as follows.

A mixture of1-methyl-3-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)urea(1.67 mmol), (R)-1-(2-chlorophenyl)ethyl(4-bromo-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (Intermediate 2A)(0.556 mmol), and sodium carbonate (1.67 mmol) in 3:1 1,4-dioxane/water(7 mL) was heated to 100° C. for 1 hour. The mixture was cooled anddiluted with water. The mixture was extracted with ethyl acetate (3×10mL). The combined organic layers were dried over anhydrous sodiumsulfate and concentrated under reduced pressure. The residue waspurified by reverse-phase HPLC to provide(R)-1-(2-chloropyridin-3-yl)ethyl(1-methyl-4-(6-(3-methylureido)pyridin-3-yl)-1H-1,2,3-triazol-5-yl)carbamate(Compound 3). (MS (m/z) 432.1 [M+H]⁺). 1H NMR (400 MHz, DMSO-d6) δ 10.05(bs, 1H), 9.41 (bs, 1H), 8.47 (d, J=2.4 Hz, 1H), 8.40 (bs, 1H),8.03-7.85 (m, 3H), 7.54 (bs, 1H), 7.42 (d, J=8.7 Hz, 1H), 5.93 (m, 1H),3.85 (s, 3H), 2.75 (d, J=4.2 Hz, 3H), 1.60 (bs, 3H).

Compound 4 was similarly prepared according to Scheme C, Step 2 byreacting (R)-1-(2-chloropyridin-3-yl)ethyl(4-bromo-1-methyl-1H-1,2,3-triazol -5-yl)carbamate (Intermediate 2B)(Example 3) with1-ethyl-3-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)ureafollowing the general process described for Compound 3 to provide(R)-1-(2-chloropyridin-3-yl)ethyl(4-(6-(3-ethylureido)pyridin-3-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 4). (MS (m/z) 444.2 [M+H]⁺). 1H NMR (400 MHz, DMSO-d6) δ 10.01(s, 1H), 9.35 (s, 1H), 8.49 (d, J=2.3 Hz, 1H), 8.09-7.81 (m, 2H),7.69-7.17 (m, 5H), 6.01 (m, 1H), 3.85 (s, 3H), 3.31-3.09 (m, 2H), 1.57(bs, 3H), 1.11 (t, J=7.2 Hz, 3H).

Example 11 Preparation of [(1R)-1-(2-chloro-3-pyridyl)ethyl]N-[5-(5-acetamido-6-fluoro-2-pyridyl)-3-methyl-triazol-4-yl]carbamate(Compound 5)

Step 1: N-(6-bromo-2-fluoro-3-pyridyl)acetamide

To a solution 6-bromo-2-fluoro-pyridin-3-amine (5.24 mmol) indichloromethane (17 mL) was added pyridine (26.2 mmol) followed byacetyl chloride (22.9 mmol). The reaction was stirred overnight. Aftercompletion of the reaction, the mixture was diluted with water. Themixture was extracted with ethyl acetate (3×10 mL). The combined organiclayers were dried over anhydrous sodium sulfate and concentrated underreduced pressure. The residue was purified by column chromatography toprovide N-(6-bromo-2-fluoro-3-pyridyl)acetamide.

Step 2:5-(5-acetamido-6-fluoro-2-pyridyl)-3-methyl-triazole-4-carboxylic acid

A mixture of N-(6-bromo-2-fluoro-3-pyridyl)acetamide (0.485 mmol),1,1′-Bis(diphenylphosphino)ferrocene-palladium(II)dichloridedichloromethane complex (0.0485 mmol), Bis(pinacolato)diboron (0.728mmol), and potassium acetate (0.728 mmol) in 1,4-dioxane (5 mL) washeated to 100° C. for 1 hour. At this point, the reaction was cooled toroom temperature, and 4-bromo-1-methyl-1H-1,2,3-triazole-5-carboxylicacid (Intermediate 1) (0.485 mmol), potassium carbonate (0.971 mmol),and water (1.5 mL) were added to the reaction. The reaction was purgedwith nitrogen and heated to 100° C. for 1 hour. After completion of thereaction, the mixture was cooled and diluted with water. The mixture wasextracted with ethyl acetate (3×10 mL). The combined organic layers weredried over anhydrous sodium sulfate and concentrated under reducedpressure. The residue was purified by reverse-phase HPLC to provide5-(5-acetamido-6-fluoro-2-pyridyl)-3-methyl-triazole-4-carboxylic acid.

Step 3: [(1R)-1-(2-chloro-3-pyridyl)ethyl]N-[5-(5-acetamido-6-fluoro-2-pyridyl)-3-methyl-triazol-4-yl]carbamate(Compound 5)

To a mixture of5-(5-acetamido-6-fluoro-2-pyridyl)-3-methyl-triazole-4-carboxylic acid(0.372 mmol), 1-propanephosphonic acid cyclic anhydride (50% in DMF,0.559 mmol), and azidotrimethysilane (0.559 mmol) acid in THF (1.9 mL)was added triethylamine (0.745 mmol) dropwise.(1R)-1-(2-chloro-3-pyridyl)ethanol (0.559 mmol) was added and the flaskwas heated at 70° C. for 1 hour. After completion of the reaction, themixture was cooled and diluted with water. The mixture was extractedwith ethyl acetate (3×10 mL). The combined organic layers were driedover anhydrous sodium sulfate and concentrated under reduced pressure.The residue was purified by reverse-phase HPLC to provide[(1R)-1-(2-chloro-3-pyridyl)ethyl]N-[5-(5-acetamido-6-fluoro-2-pyridyl)-3-methyl-triazol-4-yl]carbamate(Compound 5). (MS (m/z) 434.1 [M+H]⁺). ¹H NMR (400 MHz, Methanol-d₄) δ8.54 (dd, J=9.8, 8.3 Hz, 1H), 8.30 (s, 1H), 8.14 (s, 1H), 7.85 (d, J=8.2Hz, 1H), 7.45 (s, 1H), 6.09 (q, J=6.4 Hz, 1H), 3.96 (s, 3H), 2.21 (s,3H), 1.57 (d, J=48.3 Hz, 3H).

Example 12 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(4-aminophenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 8B)

Step 1:4-(4-((tert-butoxycarbonyl)amino)phenyl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid

To a mixture of (4-((tert-butoxycarbonyl)amino)phenyl)boronic acid (2.7mmol) and 4-bromo-1-methyl-1H-1,2,3-triazole-5-carboxylic acid(Intermediate 1) (2.4 mmol) was added potassium carbonate (7.3 mmol),and Pd(PPh₃)₄ (0.24 mmol). The mixture was suspended in 20 mL of a 10:1mixture of Dioxane/water and sparged with argon gas for 5 min. Thereaction was sealed and heated to 100° C. for 16 hours. The reaction wasdiluted with aqueous 1 M HCl, and brine, and extracted with ethylacetate (25 mL×2). The combined organics were dried over sodium sulfateand concentrated. The residue was purified by silica gel columnchromatography to provide4-(4-((tert-butoxycarbonyl)amino)phenyl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid.

Step 2: (R)-1-(2-chloropyridin-3-yl)ethyl(4-(4-((tert-butoxycarbonyl)amino)phenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

4-(4-((tert-butoxycarbonyl)amino)phenyl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid (1 mmol), 50% 1-propanephosphonic anhydride solution (1.4 mmol) inDMF, and azidotrimethylsilane (1.4 mmol), were suspended in THF (3 mL).Triethylamine (1.4 mmol) was added and the resulting solution wasallowed to stir for 30 min at room temperature.(1R)-1-(2-chloro-3-pyridyl)ethanol (1.4 mmol) was added and the mixturewas heated at reflux for 12 hours. The reaction mixture was cooled toroom temperature, and the THF was removed in vacuo. The resulting crudematerial was purified by silica gel column chromatography to provide(R)-1-(2-chloropyridin-3-yl)ethyl(4-(4-((tert-butoxycarbonyl)amino)phenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate.

Step 3: (R)-1-(2-chloropyridin-3-yl)ethyl(4-(4-aminophenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 8B)

4M HCl in 1,4-dioxane (1 mL) was added to(R)-1-(2-chloropyridin-3-yl)ethyl(4-(4-((tert-butoxycarbonyl)amino)phenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(0.5 mmol). The resulting suspension was stirred for 18 h at roomtemperature. The reaction was concentrated to afford(R)-1-(2-chloropyridin-3-yl)ethyl(4-(4-aminophenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 8B) as the hydrochloride salt.

Example 13 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(4-acetamidophenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 6)

Step 4: (R)-1-(2-chloropyridin-3-yl)ethyl(4-(4-acetamidophenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 6)

(R)-1-(2-chloropyridin-3-yl)ethyl(4-(4-aminophenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(intermediate 8B) hydrochloride salt (0.08 mmol) was dissolved indichloromethane (1 mL), pyridine (0.2 mL). Acetyl chloride (0.16 mmol)was added dropwise at room temperature. After 30 min, the reaction wasconcentrated and dissolved in tetrahydrofuran (2 mL), and 0.5 M aqueoussodium hydroxide solution (2 mL) and stirred vigorously for 10 minutes.The reaction was quenched with sat. ammonium chloride and extracted withethyl acetate (2×10 mL). The combined organics were dried over sodiumsulfate, concentrated, and purified by reverse-phase HPLC to provide(R)-1-(2-chloropyridin-3-yl)ethyl(4-(4-acetamidophenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 6). (MS (m/z) 415.08 [M+H]⁺). ¹H NMR (400 MHz, Methanol-d4) δ8.36 (s, 1H), 8.06 (s, 1H), 7.65 (s, 4H), 7.56-6.99 (m, 1H), 6.11 (s,1H), 3.95 (s, 3H), 2.17 (s, 3H), 1.82-1.19 (m, 3H).

Example 14 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(4-((methoxycarbonyl)amino)phenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 7)

(R)-1-(2-chloropyridin-3-yl)ethyl(4-(4-aminophenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 8B) hydrochloride salt (0.08 mmol) was dissolved indichloromethane (1 mL), pyridine (0.2 mL). Methyl chloroformate chloride(0.16 mmol) was added dropwise at room temperature. After 30 minutes,the reaction was concentrated and dissolved in tetrahydrofuran (2 mL),and 0.5 M aqueous sodium hydroxide solution (2 mL) and stirredvigorously for 10 minutes. The reaction was quenched with sat. ammoniumchloride, and extracted with ethyl acetate (2×10 mL). The combinedorganics were dried over sodium sulfate, concentrated, and purified byreverse-phase HPLC to provide (R)-1-(2-chloropyridin-3-yl)ethyl(4-(4-((methoxycarbonyl)amino)phenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 7). (MS (m/z) 431.1 [M+H]⁺). ¹H NMR (400 MHz, Methanol-d4) δ8.60-8.13 (m, 1H), 8.06 (s, 1H), 7.77-7.10 (m, 5H), 6.23-5.90 (m, 1H),3.96 (s, 3H), 3.78 (s, 3H), 1.80-1.38 (m, 3H).

Example 15 Preparation of (S)-2-fluoro-1-phenylethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 8D)

Step 1: tert-butyl(S)-(6-(5-(((2-fluoro-1-phenylethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyridin-3-yl)carbamate

Following the procedure described in Example 12 for the preparation of(R)-1-(2-chloropyridin-3-yl)ethyl(4-(4-((tert-butoxycarbonyl)amino)phenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,using (S)-2-fluoro-1-(3-fluorophenyl)ethan-1-ol (0.73 mmol), in place of(R)-1-(2-chloropyridin-3-yl)ethan-1-ol, tert-butyl(S)-(6-(5-(((2-fluoro-1-phenylethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyridin-3-yl)carbamatewas obtained.

Step 2: (S)-2-fluoro-1-phenylethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 8D)

4M HCl in 1,4-dioxane (1 mL) was added to tert-butyl(S)-(6-(5-(((2-fluoro-1-phenylethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyridin-3-yl)carbamate(0.34 mmol). The resulting suspension was stirred for 3 h at roomtemperature. The reaction was concentrated to afford(S)-2-fluoro-1-phenylethyl(4-(4-aminophenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 8D) as the hydrochloride salt.

Example 16 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(1-cyanocyclopropane-1-carboxamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 8)

Step 1: (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((tert-butoxycarbonyl)amino)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

To a solution of (R)-1-(2-chloropyridin-3-yl)ethyl(4-bromo-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (Intermediate 2B)(0.42 mmol) in 3 mL THF at −78° C. was added a 1 N solution of lithiumbis(trimethylsilyl)amide in THF (0.50 mmol, 1 M) dropwise. After 15minutes a 1.6 M solution of n-butyllithium (nBuLi) in hexanes (0.83mmol) was added dropwise. After 15 minutes a 1.9M solution of zincchloride (ZnCl₂) in THF (1.0 mmol) was added dropwise, and the reactionwarmed to room temperature over 20 minutes. A solution of tert-butyl(5-bromopyrazin-2-yl)carbamate (Br-pyrazine) (0.50 mmol) and(2-Dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)[2-(2′-amino-1,1′-biphenyl)]palladium(II)methanesulfonate (XPhos Pd G3) (0.042 mmol) in THF was added, and thereaction heated to 70° C. for 2 hours. The reaction was then cooled toroom temperature and quenched with saturated aqueous NH₄Cl and extractedwith EtOAc. The combined organic layers were dried over Na₂SO₄ andconcentrated. Purified by silica gel chromatography (0-20% DCM/MeOH) toprovide (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((tert-butoxycarbonyl)amino)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate.

Step 2: (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

A solution of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((tert-butoxycarbonyl)amino)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(0.126 mmol) in 4N HCl in dioxane was stirred at room temperature for 1hour. Reaction was concentrated and placed under vacuum overnight,providing (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate.

Step 3: (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(1-cyanocyclopropane-1-carboxamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 8)

A solution of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(0.0729 mmol) in 0.2 mL DMF was treated with pyridine (0.729 mmol),1-cyanocyclopropane-1-carboxylic acid (0.114 mmol) and EDC (0.0875 mmol)and stirred at room temperature for 3 hours. Diluted with aq. MeCN andpurified by RP HPLC to provide (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(1-cyanocyclopropane-1-carboxamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 27). (MS (m/z) 467.9[M+H]+). 1H NMR (400 MHz, Methanol-d4) d9.01 (s, 1H), 8.84 (s, 1H), 8.51-7.91 (m, 2H), 7.46 (s, 1H), 6.30-5.74(m, 1H), 3.97 (s, 3H), 1.84-1.38 (m, 7H).

Example 17 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-acetamido-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 9)

Step 1: N-(6-bromo-5-fluoro-3-pyridyl)acetamide

To a solution 6-bromo-5-fluoro-pyridin-3-amine (5.24 mmol) indichloromethane (17 mL) was added pyridine (26.2 mmol) followed byacetyl chloride (22.9 mmol). The reaction was stirred overnight. Aftercompletion of the reaction, the mixture was diluted with water. Themixture was extracted with ethyl acetate (3×10 mL). The combined organiclayers were dried over anhydrous sodium sulfate and concentrated underreduced pressure. The residue was purified by column chromatography toprovide 6-bromo-5-fluoro-pyridin-3-amine.

Step 2:4-(5-acetamido-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid

To a mixture of 4-bromo-1-methyl-1H-1,2,3-triazole-5-carboxylic acid(Intermediate 1) (1.3 mmol) in tetrahydrofuran (20 mL) at −78° C. wasadded a 1 M solution of lithium bis(trimethylsilyl)amide (1.3 mmol) inTHF. After 10 minutes, a 2.5 M solution of n-butyllithium (2.5 mmol) inHexanes was added. After 45 minutes, a 1.9 M solution of zinc chloride(2.5 mmol) in 2-MeTHF was added, and the reaction was warmed to roomtemperature and stirred for 30 minutes. The reaction mixture was spargedwith argon gas for 5 minutes, and thenN-(6-bromo-5-fluoro-3-pyridyl)acetamide (0.84 mmol) and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II),dichloromethane complex (0.08 mmol) were added. The reaction was heatedat 70° C. for 2 hours, after which the reaction was cooled and dilutedwith 1 M aqueous hydrogen chloride solution (20 mL). The reactionmixture was extracted with ethyl acetate (30 mL×3). The combined organiclayer was dried over sodium sulfate and concentrated to provide4-(5-acetamido-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid which was used in the next step without further purification.

Step 3: (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-acetamido-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 9)

(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-acetamido-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(0.14 mmol), 50% 1-propanephosphonic anhydride solution (0.29 mmol) inDMF, and azidotrimethylsilane (0.29 mmol), were suspended in THF (2 mL).Triethylamine (0.43 mmol) was added and the resulting solution wasallowed to stir for 30 minutes at room temperature.(1R)-1-(2-chloro-3-pyridyl)ethanol (0.29 mmol) was added and the mixturewas heated at reflux for 4 hours. The reaction mixture was cooled toroom temperature, and the THF was removed in vacuo. The resulting crudematerial was purified by reverse phase HPLC to provide(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-acetamido-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 29). (MS (m/z) 434.0 [M+H]⁺). ¹H NMR (400 MHz, Methanol-d₄) δ8.52 (s, 1H), 8.33 (s, 1H), 8.19-7.76 (m, 2H), 7.48 (s, 1H), 6.20-5.90(m, 1H), 4.01 (s, 3H), 2.21 (s, 3H), 1.60 (s, 3H).

Example 18 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-amino-4-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 7B)

Step 1: (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((tert-butoxycarbonyl)amino)-4-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

To a mixture of (R)-1-(2-chloropyridin-3-yl)ethyl(4-bromo-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,(R)-1-(2-chlorophenyl)ethyl(4-bromo-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (Intermediate 2A) (1mmol) in tetrahydrofuran (15 mL) at −78° C. was added a 1 M solution oflithium bis(trimethylsilyl)amide (1.2 mmol) in tetrahydrofuran. After 10minutes, a 2.5 M solution of n-butyllithium (2.5 mmol) in hexanes wasadded. After 45 minutes, a 1.9 M solution of zinc chloride (2.5 mmol) in2-methyl tetrahydrofuran was added, and the reaction was warmed to andstirred at room temperature for 30 minutes. The reaction mixture wassparged with argon gas for 5 minutes, and then added tert-butyl(6-chloro-4-fluoropyridin-3-yl)carbamate (1.2 mmol) and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II),dichloromethane complex (0.1 mmol). The reaction mixture was heated to70° C. for 1 hour. After completion of the reaction, the mixture wascooled and quenched with 1 N aqueous hydrochloric acid (20 mL). Theaqueous layer was extracted with ethyl acetate (3×10 mL). The combinedorganic layers were dried over anhydrous sodium sulfate and concentratedunder reduced pressure to provide (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((tert-butoxycarbonyl)amino)-4-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatewhich was used in the next step without further purification.

Step 2: (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-amino-4-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 7B)

4 M HCl in 1,4-dioxane (1 mL) was added to(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((tert-butoxycarbonyl)amino)-4-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(0.49 mmol). The resulting suspension was stirred for 4 hours at roomtemperature. The reaction was concentrated to afford(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-amino-4-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 7B) as the hydrochloride salt.

Example 19 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-acetamido-4-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 10)

The hydrochloride salt of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-amino-4-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 7B) (0.05 mmol) was dissolved in dichloromethane (1 mL)and pyridine (0.2 mL). Acetyl chloride (0.1 mmol) was added dropwise atroom temperature. After 30 minutes, the reaction was concentrated anddissolved in tetrahydrofuran (2 mL), and 1 M aqueous sodium hydroxidesolution (2 mL) and stirred vigorously for 10 minutes. The reaction wasquenched with sat. ammonium chloride and extracted with ethyl acetate(2×10 mL). The combined organics were dried over sodium sulfate,concentrated, and purified by reverse-phase HPLC to provide(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-acetamido-4-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate. (Compound 30) (MS (m/z) 434.0 [M+H]⁺). ¹H NMR (400 MHz,Methanol-d₄) δ 9.17 (d, J=9.8 Hz, 1H), 8.32 (d, J=4.4 Hz, 1H), 8.09 (s,1H), 7.79 (d, J=11.5 Hz, 1H), 7.48 (s, 1H), 6.18-6.00 (m, 1H), 3.99 (s,3H), 2.24 (s, 3H), 1.62 (s, 3H).

Example 20 Preparation of(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((tert-butoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 11)

To a mixture of4-(5-((tert-butoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid (9.4 mmol), 1-propanephosphonic acid cyclic anhydride (50% in THF,14.1 mmol), and azidotrimethysilane (14.1 mmol) acid in THF (100 mL) wasadded triethylamine (23.5 mmol) dropwise. The reaction mixture washeated at 70° C. for 1 hour followed by addition of(R)-1-(2-chloropyridin-3-yl)ethan-1-ol (18.8 mmol) at the sametemperature. After heating for 24 hours, the reaction was cooled to roomtemperature, concentrated and purified by silica gel chromatography toprovide (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((tert-butoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate.(Compound 11) (MS (m/z) 474.12 [M+H]⁺). ¹H NMR (400 MHz, Methanol-d4) δ8.67 (s, 1H), 8.31 (s, 1H), 8.08 (s, 1H), 7.94 (dd, J=8.7, 2.6 Hz, 1H),7.84 (dd, J=8.6, 0.8 Hz, 1H), 7.47 (s, 1H), 6.07 (d, J=6.7 Hz, 1H), 3.98(s, 3H), 1.75-1.46 (m, 12H).

Example 21 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5A)

4 M HCl in 1,4-dioxane (20 mL) was added to(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((tert-butoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(6.9 mmol). The resulting suspension was stirred for 18 hours at roomtemperature. The reaction was concentrated to afford(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5A) as the hydrochloride salt.

Example 22 Preparation of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5B)

Step 1: tert-butyl(R)-(6-(5-(((1-(2,5-difluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyridin-3-yl)carbamate

To a mixture of4-(5-((tert-butoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid (10.6 mmol), 1-propanephosphonic acid cyclic anhydride (50% in THF,16 mmol), and azidotrimethysilane (16 mmol) acid in THF (15 mL) wasadded triethylamine (27 mmol) dropwise. The reaction mixture was heatedat 70° C. for 0.5 hour followed by addition of(R)-1-(2,5-difluoropyridin-3-yl)ethan-1-ol (21 mmol) at the sametemperature. After heating for 24 hours, the reaction was cooled to roomtemperature, concentrated and purified by silica gel chromatography toprovide tert-butyl(R)-(6-(5-(((1-(2,5-difluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyridin-3-yl)carbamate.

Step 2: (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5B)

4 M HCl in 1,4-dioxane (15 mL) was added to tert-butyl(R)-(6-(5-(((1-(2,5-difluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyridin-3-yl)carbamate(4.2 mmol). The resulting suspension was stirred for 18 hours at roomtemperature. The reaction was concentrated to afford(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5B) as the hydrochloride salt.

Example 23 Preparation of (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5C)

Following the procedure described in Example 22 for the preparation of(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5B), using (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethan-1-ol(1.7 mmol), in place of (R)-1-(2,5-difluoropyridin-3-yl)ethan-1-ol,(R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5C) was obtained.

Example 24 Preparation of (R)-1-(2-fluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5D)

Following the procedure described in Example 22 for the preparation of(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5B), using (R)-1-(2-fluoropyridin-3-yl)ethan-1-ol (7.0mmol), in place of (R)-1-(2,5-difluoropyridin-3-yl)ethan-1-ol,(R)-1-(2-fluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5D) was obtained.

Example 25 Preparation of (R)-1-(5-fluoro-2-methylpyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5E)

Following the procedure described in Example 22 for the preparation of(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5B), using (R)-1-(5-fluoro-2-methylpyridin-3-yl)ethan-1-ol(6.4 mmol), in place of (R)-1-(2,5-difluoropyridin-3-yl)ethan-1-ol,(R)-1-(5-fluoro-2-methylpyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5E) was obtained.

Example 26 Preparation of (R)-1-(2-chlorophenyl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 6A)

Following the procedure described in Example 22 for the preparation of(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5B), using (R)-1-(2-chlorophenyl)ethan-1-ol (3.2 mmol), inplace of (R)-1-(2,5-difluoropyridin-3-yl)ethan-1-ol,(R)-1-(2-chlorophenyl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 6A) was obtained.

Example 27 Preparation of (S)-2-fluoro-1-(3-fluorophenyl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 6B)

Following the procedure described in Example 22 for the preparation of(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5B), using (S)-2-fluoro-1-(3-fluorophenyl)ethan-1-ol (2.3mmol), in place of (R)-1-(2,5-difluoropyridin-3-yl)ethan-1-ol,(S)-2-fluoro-1-(3-fluorophenyl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 6B) was obtained.

Example 28 Preparation of 1-(2-chloro-6-fluoropyridin-3-yl)ethan-1-ol

2-Chloro-6-fluoronicotinaldehyde (2.51 mmol) dissolved in methyltetrahydrofuran (20 mL) was cooled in an ice/acetonitrile bath and thenmethylmagnesium bromide solution (3.0 M, 7.20 mmol) was added dropwise.The reaction mixture was quenched with addition of ethanol, and thendiluted with ethyl acetate and washed with 10% citric acid. The organiclayer was concentrated. The residue was purified by columnchromatography to give 1-(2-chloro-6-fluoropyridin-3-yl)ethan-1-ol.

Example 29 Preparation of 1-(2-fluoro-5-methylpyridin-4-yl)ethan-1-ol

A solution of 2-fluoro-4-iodo-5-methylpyridine (4.22 mmol) in 20 mL THFwas cooled to 0° C. and treated with 1.6 M nBuLi in hexanes (5.06 mmol).After 15 min DMF (12.7 mmol) was added dropwise. The reaction wasstirred for 30 min, then warmed to room temperature and quenched withsat NH₄Cl. The mixture was extracted with EtOAc, dried with MgSO₄ andconcentrated to provide 2-fluoro-5-methylisonicotinaldehyde.2-fluoro-5-methylisonicotinaldehyde (5.5 mmol) was taken up in 25 mL THFand cooled to −15° C. in an ice-acetone bath. Treated with 3 M MeMgBr inTHF (11.2 mmol) and stirred for 20 minutes. Quenched with sat NH₄Cl andextracted with EtOAc, dried with MgSO₄, filtered and concentrated toprovide 1-(2-fluoro-5-methylpyridin-4-yl)ethan-1-ol (MS (m/z) 155.9[M+H]+).

Example 30 Preparation of 1-(2,5-difluoropyridin-4-yl)ethan-1-ol

Following the procedure described in Example 29 for the synthesis of1-(2-fluoro-5-methylpyridin-4-yl)ethan-1-ol, using2,5-difluoroisonicotinaldehyde (11.9 mmol) in place of2-fluoro-5-methylisonicotinaldehyde,1-(2,5-difluoropyridin-4-yl)ethan-1-ol was obtained. (MS (m/z)160.11[M+H]+).

Example 31 Preparation of 1-(5-bromo-2-fluoropyridin-3-yl)ethan-1-ol

Following the procedure described in Example 29 for the synthesis of1-(2-fluoro-5-methylpyridin-4-yl)ethan-1-ol, using5-bromo-2-fluoronicotinaldehyde (7.35 mmol) in place of2-fluoro-5-methylisonicotinaldehyde,1-(5-bromo-2-fluoropyridin-3-yl)ethan-1-ol was obtained. (MS (m/z)220.01[M+H]+).

Example 32 Preparation of 1-(5-bromo-2-chloropyridin-3-yl)ethan-1-ol

Following the procedure described in Example 29 for the synthesis of1-(2-fluoro-5-methylpyridin-4-yl)ethan-1-ol, using5-bromo-2-chloronicotinaldehyde (10.6 mmol) in place of2-fluoro-5-methylisonicotinaldehyde,1-(5-bromo-2-chloropyridin-3-yl)ethan-1-ol was obtained. (MS (m/z)235.99[M+H]+).

Example 33 Preparation of 1-(2,5-difluoropyridin-4-yl)ethan-1-ol

Following the procedure described in Example 29 for the synthesis of1-(2-fluoro-5-methylpyridin-4-yl)ethan-1-ol, using5-bromo-2-fluoronicotinaldehyde (7.4 mmol) in place of2-fluoro-5-methylisonicotinaldehyde,1-(5-bromo-2-fluoropyridin-3-yl)ethan-1-ol. (MS (m/z) 220.01 [M+H]+).

Example 34 Preparation of 1-(2-chloro-6-fluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5F)

Following the procedure described in Example 22 for the preparation of(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5B), using 1-(2-chloro-6-fluoropyridin-3-yl)ethan-1-ol(0.34 mmol), in place of (R)-1-(2,5-difluoropyridin-3-yl)ethan-1-ol,1-(2-chloro-6-fluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5F) was obtained.

Example 35 Preparation of 1-(5-bromo-2-fluoropyridin-3-yl)ethyl(1-methyl-4-(5-(2,2,2-trifluoroacetamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate(Compound 12)

Step 1: tert-butyl(6-(5-(((1-(5-bromo-2-fluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyridin-3-yl)carbamate

A solution of tert-butyl(6-(5-(((1-(5-bromo-2-fluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyridin-3-yl)carbamate(0.125 mmol) in 0.2 mL THF was treated with T3P (0.25 mmol),trimethylsilyl-azide (TMS-N3) (0.25 mmol) and triethylamine (TEA) (0.25mmol) and stirred at room temperature for 20 minutes. A solution of1-(5-bromo-2-fluoropyridin-3-yl)ethan-1-ol in 200 μL THF was added andthe mixture heated at 65° C. for 90 minutes. The mixture was thendiluted with DCM and washed with aq. NaHCO3. Purified by silica gelchromatography to provide tert-butyl(6-(5-(((1-(5-bromo-2-fluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyridin-3-yl)carbamate.

Step 2: 2,2,2-trifluoroacetic acid,6-(5-(((1-(5-bromo-2-fluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyridin-3-aminiumsalt

Tert-butyl(6-(5-(((1-(5-bromo-2-fluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyridin-3-yl)carbamate(0.125 mmol) was taken up in 2 mL DCM and 2 mL trifluoroacetic acid(TFA). Stirred for 5 minutes then concentrated. Taken up in 15 mLdichloroethane and concentrated again. This was repeated 2 times, andthe resulting oil left under high vacuum overnight. The obtained2,2,2-trifluoroacetic acid,6-(5-(((1-(5-bromo-2-fluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyridin-3-aminiumsalt used crude in the next step.

Step 3: 1-(5-bromo-2-fluoropyridin-3-yl)ethyl(1-methyl-4-(5-(2,2,2-trifluoroacetamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate(Compound 12)

2,2,2-Trifluoroacetic acid,6-(5-(((1-(5-bromo-2-fluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyridin-3-aminiumsalt (0.125 mmol) taken up in 2 mL DCM and cooled to 0° C. This solutionwas treated with pyridine (0.36 mmol) and methanesulfonic anhydride(0.156 mmol). Allowed to warm to room temperature and stir for 30minutes. The reaction was concentrated and the residue taken up in MeCNand water. Purification by RP HPLC provided1-(5-bromo-2-fluoropyridin-3-yl)ethyl(1-methyl-4-(5-(2,2,2-trifluoroacetamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate.(Compound 12) (MS (m/z) 532.04 [M+H]+). 1H NMR (400 MHz, DMSO-d6) δ10.08 (s, 1H), 9.85 (m, 1H), 8.37-8.32 (m, 1H), 7.95 (d, J=8.6 Hz, 1H),7.69 (dd, J=8.6, 2.7 Hz, 1H), 5.80 (s, 1H), 3.89 (s, 3H), 3.08 (s, 3H),1.77-1.38 (m, 3H).

Example 36 Preparation of 1-(5-bromo-2-chloropyridin-3-yl)ethyl(1-methyl-4-(5-(2,2,2-trifluoroacetamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate(Compound 13)

Following the procedure described in Example 35 for the synthesis of1-(5-bromo-2-fluoropyridin-3-yl)ethyl(1-methyl-4-(5-(2,2,2-trifluoroacetamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate,using 1-(5-bromo-2-chloropyridin-3-yl)ethan-1-ol (0.143 mmol) in placeof 1-(5-bromo-2-fluoropyridin-3-yl)ethan-1-ol,1-(5-bromo-2-chloropyridin-3-yl)ethyl(1-methyl-4-(5-(2,2,2-trifluoroacetamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamatewas obtained (Compound 13). (MS (m/z) 548.03 [M+H]+). 1H NMR (400 MHz,DMSO-d6) δ 11.54 (s, 1H), 9.94 (s, 1H), 8.81 (s, 1H), 8.54 (s, 1H), 8.12(dd, J=8.6, 2.6 Hz, 1H), 8.02 (d, J=8.6 Hz, 1H), 7.38 (s, 1H), 5.84 (s,1H), 3.91 (s, 3H), 1.58 (s, 3H).

Example 37 Preparation of (R)-1-(5-chloro-2-fluoropyridin-3-yl)ethyl(4-(5-acetamidopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 14)

Step 1:(R)-1-(5-chloro-2-fluoropyridin-3-yl)ethyl(4-(5-((tert-butoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

Following the procedure described in Example 35, step 1 for thesynthesis of 1-(5-bromo-2-fluoropyridin-3-yl)ethyl(1-methyl-4-(5-(2,2,2-trifluoroacetamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate,using (R)-1-(5-chloro-2-fluoropyridin-3-yl)ethan-1-ol (0.43 mmol) inplace of 1-(5-bromo-2-fluoropyridin-3-yl)ethan-1-ol,(R)-1-(5-chloro-2-fluoropyridin-3-yl)ethyl(4-(5-((tert-butoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatewas obtained. (MS (m/z) 492.03 [M+H]+).

Step 2: (R)-1-(5-chloro-2-fluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride

A solution of (R)-1-(5-chloro-2-fluoropyridin-3-yl)ethyl(4-(5-((tert-butoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(0.193 mmol) in 4N HCl in dioxane was stirred at room temperature for 1hour. Reaction was concentrated and placed under vacuum overnight,providing (R)-1-(5-chloro-2-fluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride as an oil.

Step 3: (R)-1-(5-chloro-2-fluoropyridin-3-yl)ethyl(4-(5-acetamidopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 14)

A solution of (R)-1-(5-chloro-2-fluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (0.193 mmol) in 0.5 mL DCM was treated with pyridine (2.9mmol) and cooled to 0° C. Acetyl chloride (0.212 mmol) was added and themixture stirred at 0° C. for 45 minutes. Reaction was concentrated invacuo and purified by RP HPLC to provide(R)-1-(5-chloro-2-fluoropyridin-3-yl)ethyl(4-(5-acetamidopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate.(Compound 14) (MS (m/z) 434.0 [M+H]+). H NMR (400 MHz, Acetonitrile-d3)δ 8.98-8.93 (m, 1H), 8.76 (s, 1H), 8.27 (d, J=3.0 Hz, 1H), 8.24-8.14 (m,1H), 8.04 (d, J=8.7 Hz, 1H), 7.81 (ddd, J=9.0, 3.1, 0.7 Hz, 1H), 3.97(s, 3H), 2.16 (s, 3H), 1.62-1.55 (m, 3H).

Example 38 Preparation of (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-acetamidopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 15)

Following the procedure described in Example 39, step 3 for thesynthesis of (R)-1-(5-chloro-2-fluoropyridin-3-yl)ethyl(4-(5-acetamidopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,using (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (0.23mmol) in place of (R)-1-(5-chloro-2-fluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,(R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-acetamidopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 15) was obtained. (MS (m/z) 434.0 [M+H]+) H NMR (400 MHz,Acetonitrile-d3) δ 8.98-8.93 (m, 1H), 8.76 (s, 1H), 8.27 (d, J=3.0 Hz,1H), 8.24-8.14 (m, 1H), 8.04 (d, J=8.7 Hz, 1H), 7.81 (ddd, J=9.0, 3.1,0.7 Hz, 1H), 3.97 (s, 3H), 2.16 (s, 3H), 1.62-1.55 (m, 3H).

Example 39 Preparation of (R)-1-(2-chloropyridin-3-4)ethyl(4-(5-formamidopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 16)

To the acetic anhydride (3 mmol) at room temperature under an argonatmosphere was added formic acid (5 mmol). The reaction mixture wasstirred at room temperature for 30 minutes. Then(R)-1-(2-chloropyridin-3-yl) ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl) carbamatehydrochloride (Intermediate 5A) (0.37 mmol) in THF (0.33 mL) at roomtemperature was added to the reaction mixture. The reaction mixture wasstirred at 60° C. for 1 hour. The reaction mixture was concentrated todryness and then co-evaporated with toluene. The residue was purified byreverse-phase HPLC to provide (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-formamidopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate.(Compound 41) (MS (m/z) 402.0 [M+H]⁺). ¹H NMR (400 MHz, Methanol-d₄) δ8.89 (d, 1H), 8.37 (d, 2H), 8.19-8.03 (m, 1H), 8.02-7.89 (m, 1H),7.80-7.59 (m, 1H), 7.49 (s, 1H), 6.09 (m, 1H), 4.00 (d, 3H), 1.63 (s,3H).

Example 40 Preparation of(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((methoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 17)

(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride salt (Intermediate 5A) (0.78 mmol) was dissolved indichloromethane (1 mL), pyridine (0.2 mL). Methyl chloroformate chloride(0.14 mmol) was added dropwise at room temperature. After 30 minutes,the reaction was concentrated and dissolved in tetrahydrofuran (2 mL),and 0.5 M aqueous sodium hydroxide solution (2 mL) and stirredvigorously for 10 minutes. The reaction was quenched with sat. ammoniumchloride, and extracted with ethyl acetate (2×10 mL). The combinedorganics were dried over sodium sulfate, concentrated, and purified byreverse-phase HPLC to provide (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((methoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate. (Compound 17) (MS (m/z) 432.1 [M+H]⁺). ¹H NMR (400 MHz,Methanol-d₄) δ 8.70 (s, 1H), 8.31 (s, 1H), 8.13-7.92 (m, 2H), 7.87 (d,J=8.4 Hz, 1H), 7.46 (s, 1H), 6.21-5.92 (m, 1H), 3.98 (s, 3H), 3.81 (s,3H), 1.61 (s, 3H).

Example 41 Preparation of (S)-2-fluoro-1-phenylethyl(4-(4-((methoxycarbonyl)amino)phenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 18)

Following the procedure described in Example 40 for the synthesis of(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((methoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,using (S)-2-fluoro-1-phenylethyl(4-(4-aminophenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 8D) (0.06 mmol) in place of(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,(S)-2-fluoro-1-phenylethyl(4-(4-((methoxycarbonyl)amino)phenyl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatewas obtained. (Compound 18) (MS (m/z) 414.1 [M+H]⁺). ¹H NMR (400 MHz,Methanol-d₄) δ 7.87-6.82 (m, 9H), 6.03 (s, 1H), 4.81-4.56 (m, 2H), 3.92(s, 3H), 3.78 (s, 3H).

Example 42 Preparation of (S)-2-fluoro-1-(3-fluorophenyl)ethyl(4-(5-((methoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 19)

Following the procedure described in Example 40 for the synthesis of(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((methoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,using (S)-2-fluoro-1-(3-fluorophenyl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 6B) (0.05 mmol) in place of(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,(S)-2-fluoro-1-(3-fluorophenyl)ethyl(4-(5-((methoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatewas obtained. (Compound 19) (MS (m/z) 433.2 [M+H]⁺). ¹H NMR (400 MHz,Methanol-d₄) δ 8.69 (s, 1H), 8.01 (d, J=8.3 Hz, 1H), 7.84 (d, J=8.7 Hz,1H), 7.57-6.62 (m, 4H), 6.09-5.77 (m, 1H), 4.80-4.47 (m, 2H), 3.97 (s,3H), 3.79 (s, 3H).

Example 43 Preparation of(R)-1-(2-chlorophenyl)ethyl(4-(5-((methoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 20)

Following the procedure described in Example 40 for the synthesis of(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((methoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,using (R)-1-(2-chlorophenyl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 6A) (0.03 mmol) in place of(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,(R)-1-(2-chlorophenyl)ethyl(4-(5-((methoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 20) was obtained. (MS (m/z) 431.2 [M+H]⁺). ¹H NMR (400 MHz,Methanol-d₄) δ 8.74 (s, 1H), 8.02 (d, J=7.6 Hz, 1H), 7.83 (d, J=8.7 Hz,1H), 7.74-7.00 (m, 4H), 6.14 (d, J=6.7 Hz, 1H), 3.96 (s, 3H), 3.79 (s,3H), 1.42 (s, 3H).

Example 44 Preparation of(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((ethoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 21)

(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride salt (Intermediate 5A) (0.10 mmol) suspended indichloromethane (1 mL) was treated with N,N-diisopropylethylamine (30μL, 0.17 mmol) followed by ethyl chloroformate (0.210 mmol). Thereaction mixture was stirred at room temperature for 15 minutes. Thereaction mixture was concentrated. The residue was purified on the HPLCand the fractions were dried by a lyophilizer. The lyophilized solid wasdissolved in dissolved in methyl tetrahydrofuran (1 mL) and treated with1N sodium hydroxide solution (400 μL). The reaction mixture was heatedat 55° C. for 30 minutes. After cooling to room temperature, thereaction mixture was concentrated. The residue was purified on the HPLCto provide (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((ethoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 21). (MS (m/z) 446.0 [M+H]⁺). ¹H NMR (400 MHz, Methanol-d₄) δ8.80 (s, 1H), 8.34 (s, 1H), 8.06 (d, J=8.7 Hz, 2H), 7.89 (d, J=8.7 Hz,1H), 7.51 (s, 1H), 6.08 (d, J=6.9 Hz, 1H), 4.27 (q, J=7.1 Hz, 2H), 4.00(s, 3H), 1.65 (s, 3H), 1.36 (t, J=7.1 Hz, 3H).

Example 45 Preparation of(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((isobutoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 22)

Following the procedure described in Example 44 for the synthesis of(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((ethoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,using isobutyl chloroformate (0.2 mmol) in place of methylchloroformate, (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((isobutoxycarbonyl)amino)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 22) was obtained. (MS (m/z) 474.1 [M+H]⁺). ¹H NMR (400 MHz,Methanol-d₄) δ 8.84 (s, 1H), 8.34 (s, 1H), 8.09 (d, J=8.9 Hz, 2H), 7.90(d, J=8.6 Hz, 1H), 7.51 (s, 1H), 6.09 (d, J=7.1 Hz, 1H), 4.01 (d, J=6.7Hz, 2H), 4.00 (s, 4H), 2.04 (dq, J=13.4, 6.7 Hz, 1H), 1.65 (s, 3H), 1.03(d, J=6.7 Hz, 6H).

Example 46 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-acetamidopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 23)

The hydrochloride salt of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5A) (0.07 mmol) was dissolved in dichloromethane (1 mL)and pyridine (0.2 mL). Acetyl chloride (0.14 mmol) was added dropwise atroom temperature. After 30 min, the reaction was concentrated anddissolved in tetrahydrofuran (2 mL), and 1 M aqueous sodium hydroxidesolution (2 mL) and stirred vigorously for 10 minutes. The reaction wasquenched with sat. ammonium chloride, and extracted with ethyl acetate(2×10 mL). The combined organics were dried over sodium sulfate,concentrated, and purified by reverse-phase HPLC to provide(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-acetamidopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate.(Compound 23) (MS (m/z) 416.1 [M+H]⁺). ¹H NMR (400 MHz, Methanol-d₄) δ8.83 (s, 1H), 8.31 (s, 1H), 8.21-7.95 (m, 2H), 7.89 (d, J=8.6 Hz, 1H),7.46 (s, 1H), 6.08 (m, 1H), 3.98 (s, 3H), 2.20 (s, 3H), 1.61 (s, 3H).

Example 47 Preparation of (R)-1-(2-chlorophenyl)ethyl(4-(5-acetamidopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 24)

Following the procedure described in Example 46 for the synthesis of(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-acetamidopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,using (R)-1-(2-chlorophenyl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 6A) (0.03 mmol) in place of(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,(R)-1-(2-chlorophenyl)ethyl(4-(5-acetamidopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatewas obtained (Compound 24). (MS (m/z) 415.2 [M+H]⁺). ¹H NMR (400 MHz,Methanol-d₄) δ 8.88 (s, 1H), 8.10 (dd, J=8.6, 2.6 Hz, 1H), 7.86 (d,J=8.6 Hz, 1H), 7.71-7.05 (m, 4H), 6.29-5.90 (m, 1H), 3.96 (s, 3H), 2.18(s, 3H), 1.55 (s, 3H).

Example 48 Preparation of (S)-2-fluoro-1-(3-fluorophenyl)ethyl(4-(5-acetamidopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 25)

Following the procedure described in Example 46 for the synthesis of(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-acetamidopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,using (S)-2-fluoro-1-(3-fluorophenyl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 6B) (0.05 mmol) in place of(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,(S)-2-fluoro-1-(3-fluorophenyl)ethyl(4-(5-acetamidopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate.(Compound 25) (MS (m/z) 417.2 [M+H]⁺). 1H NMR (400 MHz, Methanol-d4) δ8.89 (s, 1H), 8.12 (dd, J=8.8, 2.4 Hz, 1H), 7.87 (d, J=8.7 Hz, 1H),7.56-6.58 (m, 4H), 6.11-5.70 (m, 1H), 4.79-4.30 (m, 2H), 3.98 (s, 3H),2.18 (s, 3H).

Example 49 Preparation of 1-(2-fluoro-5-methylpyridin-4-yl)ethyl(4-(5-(3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 26)

Step 1: methyl4-(5-(3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylate

To a mixture of methyl4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylatehydrochloride (Intermediate 3A) (4.3 mmol) in a 5:1 mixture ofDCM:pyridine (25 mL) was added 3,3-difluorocyclobutane-1-carboxylic acid(5.1 mmol) and N-Ethyl-N′-(3-dimethylaminopropyl) carbodiimidehydrochloride (5.1 mmol). The reaction mixture was left with magneticstirring for 2 hours at which point, the reaction was concentrated toprovide the crude methyl4-(5-(3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylatewhich was used directly in the next step.

Step 2:4-(5-(3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid

Crude methyl4-(5-(3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylate(4.3 mmol) was treated with with 2 M aqueous NaOH (50 mL), and THF (25mL) and stirred vigorously for 30 minutes. Next, the reaction wastreated with conc. HCl until pH=5. The precipitate was filtered anddried under vacuum to provide4-(5-(3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid which was used in the next step without further purification.

Step 3: 1-(2-fluoro-5-methylpyridin-4-yl)ethyl(4-(5-(3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 26)

A solution of4-(5-(3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid (0.0889 mmol) in 100 □L DMF was treated with 50% T3P in DMF (0.178mmol) TMS-N3 (0.156 mmol) and TEA (0.267 mmol) and the mixture stirredfor 20 minutes. 1-(2-fluoro-5-methylpyridin-4-yl)ethan-1-ol (0.156 mmol)was added and the reaction heated at 65° C. for 2 hours. The reactionwas cooled to rt and purified by RP HPLC to provide1-(2-fluoro-5-methylpyridin-4-yl)ethyl(4-(5-(3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 26). (MS (m/z) 490.04) [M+H]+) 1H NMR (400 MHz,Acetonitrile-d3) δ 9.00-8.89 (m, 1H), 8.88-8.75 (m, 1H), 8.55 (s, 1H),8.20 (ddt, J=9.1, 5.8, 2.8 Hz, 1H), 8.07-7.97 (m, 2H), 7.06 (s, 1H),5.90 (q, J=6.7 Hz, 1H), 3.96 (s, 3H), 3.18-3.06 (m, 1H), 3.02-2.79 (m,3H), 2.31 (s, 3H), 2.10 (m, 1H), 1.53 (d, J=6.7 Hz, 3H).

Example 50 Preparation of 1-(2-fluoro-5-methylpyridin-4-yl)ethyl(4-(5-(1-cyanocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 27)

Step 1: methyl4-(5-(1-cyanocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylate

Following the procedure described in Example 49, step 1 for thesynthesis methyl4-(5-(3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylate,using 1-cyanocyclopropane-1-carboxylic acid (5.1 mmol) in place of3,3-difluorocyclobutane-1-carboxylic acid, methyl4-(5-(1-cyanocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylatewas obtained.

Step 2:4-(5-(1-cyanocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid

Following the procedure described in Example 49, step 2 for thesynthesis4-(5-(3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid, using methyl4-(5-(1-cyanocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylate(5.1 mmol) in place of methyl4-(5-(3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylate,4-(5-(1-cyanocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid was obtained.

Step 3:1-(2-fluoro-5-methylpyridin-4-yl)ethyl(4-(5-(1-cyanocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 27)

Following the procedure described in Example 49, step 3 for thesynthesis of 1-(2-fluoro-5-methylpyridin-4-yl)ethyl(4-(5-(3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,using4-(5-(1-cyanocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid (0.0961 mmol) in place of4-(5-(3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid,4-(5-(3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid was obtained (Compound 27). (MS (m/z) 465.12 [M+H]+). 1H NMR (400MHz, Acetonitrile-d3) δ 9.00-8.89 (m, 1H), 8.88-8.75 (m, 1H), 8.55 (s,1H), 8.20 (ddt, J=9.1, 5.8, 2.8 Hz, 1H), 8.07-7.97 (m, 2H), 7.06 (s,1H), 5.90 (q, J=6.7 Hz, 1H), 3.96 (s, 3H), 3.18-3.06 (m, 1H), 3.02-2.79(m, 3H), 2.31 (s, 3H), 2.10 (m, 1H), 1.53 (d, J=6.7 Hz, 3H).

Example 51 Preparation of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 28)

To a mixture of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5B) (0.07 mmol) in pyridine (0.5 mL) was added3,3-difluorocyclobutanecarbonyl chloride (0.07 mmol). The reactionmixture was left with magnetic stirring for 2 hours at which point water(1 mL) was added the crude mixture was purified by HPLC to provide(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 28). (MS (m/z) 494.1 [M+H]⁺). 1H NMR (400 MHz, Methanol-d4) δ8.79 (s, 1H), 8.21-7.67 (m, 4H), 5.95 (s, 1H), 4.00 (s, 3H), 3.21-3.05(m, 1H), 3.05-2.68 (m, 4H), 1.62 (s, 3H).

Example 52 Preparation of Compounds 29 to 37

Compounds 29 to 37 were generally synthesized according Scheme C, Step4. For example, (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-benzamidopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 29) was prepared as follows.

To a mixture of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (Intermediate 5A) (0.07 mmol) in pyridine (0.5 mL) wasadded benzoyl chloride (0.07 mmol). The reaction mixture was left withmagnetic stirring for 2 h at which point water (1 mL) was added thecrude mixture was purified by HPLC to provide(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-benzamidopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 29). (MS (m/z) 478.1 [M+H]⁺). ¹H NMR (400 MHz, Methanol-d₄) δ9.02 (s, 1H), 8.46-7.88 (m, 6H), 7.88-7.01 (m, 4H), 6.09 (q, J=6.6 Hz,1H), 3.99 (s, 3H), 1.62 (s, 3H).

Compounds 30-37 (Table 1) were similarly prepared according to Scheme C,Step 4 by reacting (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5A) (Example 21) with a Reagent listed in Table 1following the general process described for Compound 29.

TABLE 1 Compounds prepared according to Scheme C, Step 4. LCMS CompoundNo. Structure Reagent m/z 1H NMR Compound 29(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-benzamidopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5- yl)carbamate

478.1 1H NMR (400 MHz, Methanol-d4) δ 9.02 (s, 1H), 8.46-7.88 (m, 6H),7.88-7.01 (m, 4H), 6.09 (q, J = 6.6 Hz, 1H), 3.99 (s, 3H), 1.62 (s, 3H).Compound 30 (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-butyramidopyridin-2-yl)-1- methyl-1H-1,2,3-triazol-5- yl)carbamate

444.1 1H NMR (400 MHz, Methanol-d4) δ 8.85 (s, 1H), 8.53-7.71 (m, 4H),7.46 (s, 1H), 6.08 (d, J = 7.1 Hz, 1H), 3.99 (s, 3H), 2.43 (t, J = 7.4Hz, 2H), 1.88-1.23 (m, 5H), 1.05 (t, J = 7.4 Hz, 3H). Compound 31(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(2-methoxyacetamido)pyridin-2-yl)-1- methyl-1H-1,2,3-triazol-5-yl)carbamate

446.1 1H NMR (400 MHz, Methanol-d4) δ 8.92 (s, 1H), 8.51-7.79 (m, 4H),7.47 (s, 1H), 6.08 (d, J = 6.5 Hz, 1H), 4.12 (d, J = 2.5 Hz, 2H), 3.99(d, J = 2.6 Hz, 3H), 3.54 (d, J = 2.5 Hz, 3H), 1.90-1.23 (m, 3H).Compound 32 (R)-1-(2-chloropyridin-3-yl)ethyl (1-methyl-4-(5-(1-methylcyclopropane-1- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

456.2 1H NMR (400 MHz, Methanol-d4) δ 8.85 (s, 1H), 8.53-7.69 (m, 4H),7.46 (s, 1H), 6.08 (d, J = 6.8 Hz, 1H), 3.98 (s, 3H), 1.51 (s, 6H), 1.27(q, J = 3.8 Hz, 2H), 0.82-0.73 (m, 2H). Compound 33(R)-1-(2-chloropyridin-3-yl)ethyl (1-methyl-4-(5-propionamidopyridin-2-yl)-1H- 1,2,3-triazol-5-yl)carbamate

430.1 1H NMR (400 MHz, Methanol-d4) δ 8.84 (s, 1H), 8.49-7.71 (m, 4H),7.44 (dd, J = 7.7, 4.7 Hz, 1H), 6.08 (d, J = 6.6 Hz, 1H), 3.99 (s, 3H),2.47 (q, J = 7.6 Hz, 2H), 1.84-1.38 (m, 3H), 1.25 (t, J = 7.6 Hz, 3H).Compound 34 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(cyclopropanecarboxamido)pyridin- 2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

442.1 1H NMR (400 MHz, Methanol-d4) δ 8.84 (s, 1H), 8.53-7.73 (m, 4H),7.44 (dd, J = 7.7, 4.7 Hz, 1H), 6.08 (d, J = 6.7 Hz, 1H), 3.98 (s, 3H),1.83 (tt, J = 7.9, 4.6 Hz, 1H), 1.78-1.35 (m, 3H), 0.98 (ddt, J = 34.8,8.0, 2.9 Hz, 4H). Compound 35 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(cyclobutanecarboxamido)pyridin- 2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

456.2 1H NMR (400 MHz, Methanol-d4) δ 8.85 (s, 1H), 8.55-7.76 (m, 4H),7.44 (dd, J = 7.7, 4.8 Hz, 1H), 6.08 (d, J = 6.9 Hz, 1H), 3.98 (s, 3H),2.51-2.33 (m, 2H), 2.26 (dddd, J = 10.2, 8.6, 6.8, 3.3 Hz, 2H),2.17-2.02 (m, 1H), 2.02-1.88 (m, 1H), 1.57 (d, J = 31.9 Hz, 3H).Compound 36 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(2,2-difluoroacetamido)pyridin-2-yl)-1- methyl-1H-1,2,3-triazol-5-yl)carbamate

452.1 1H NMR (400 MHz, Methanol-d4) δ 8.93 (s, 1H), 8.43-7.72 (m, 4H),7.47 (s, 1H), 6.52-5.83 (m, 2H), 3.99 (s, 3H), 1.58 (d, J = 26.9 Hz,3H). Compound 37 (R)-1-(2-chloropyridin-3- yl)ethyl (4-(5-(3,3-difluorocyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5- yl)carbamate

492.2 1H NMR (400 MHz, Methanol-d4) δ 8.85 (s, 1H), 8.53-7.72 (m, 4H),7.47 (s, 1H), 6.07 (d, J = 6.5 Hz, 1H), 3.99 (s, 3H), 3.15 (pd, J = 8.4,3.2 Hz, 1H), 3.05-2.69 (m, 4H), 1.61 (s, 3H).

Example 53 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(azetidine-3-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 38)

To a mixture of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (Intermediate 5A) (0.06 mmol) in pyridine (0.5 mL) wasadded 1-Boc-azetidine-3-carboxylic acid (0.067 mmol) andN-Ethyl-N′-(3-dimethylaminopropyl) carbodiimide hydrochloride (0.064mmol). The reaction mixture was left with magnetic stirring for 2 hoursat which point it was concentrated in vacuo and trifluoroacetic acid(0.2 mL) was added. The reaction mixture was left with magnetic stirringfor 0.5 h at which point water (1 mL) and pyridine (0.5 mL) was addedthe crude mixture was purified by HPLC to provide(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(azetidine-3-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 38). (MS (m/z) 457.1 [M+H]⁺). ¹H NMR (400 MHz, Methanol-d₄) δ8.86 (s, 1H), 8.61-7.76 (m, 4H), 7.59 (d, J=90.0 Hz, 1H), 6.07 (s, 1H),4.53-4.18 (m, 4H), 4.00 (s, 3H), 3.87 (tt, J=8.9, 7.1 Hz, 1H), 1.66 (d,J=36.7 Hz, 3H).

Example 54 Preparation of Compounds 39 to 184 and 195 to 296

Compounds 39 to 184 and 195 to 296 were generally synthesized accordingScheme C, Step 4. For example,(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(1-cyanocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (Compound 39) wasprepared as follows.

To a mixture of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (Intermediate 5B) (0.06 mmol) in pyridine (0.5 mL) wasadded 1-cyanocyclopropane-1-carboxylic acid (0.067 mmol) andN-Ethyl-N′-(3-dimethylaminopropyl) carbodiimide hydrochloride (0.067mmol). The reaction mixture was left with magnetic stirring for 2 hoursat which point water (1 mL) was added the crude mixture was purified byHPLC to provide (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(1-cyanocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 39). (MS (m/z) 469.1 [M+H]⁺). ¹H NMR (400 MHz, Methanol-d₄) δ8.79 (s, 1H), 8.33-7.46 (m, 4H), 5.95 (d, J=6.9 Hz, 1H), 4.00 (s, 3H),1.82-1.36 (m, 7H).

Compounds 40-160 and 195-206 (Table 2) were similarly prepared accordingto Scheme C, Step 4 by reacting (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,Intermediate 5A (Example 21) with the Reagent listed in Table 2 in placeof 1-cyanocyclopropane-1-carboxylic acid following the general processdescribed for Compound 39.

To a mixture of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (Intermediate 5B) (0.073 mmol) in pyridine (1.0 mL) wasadded 2-(trifluoromethyl)pyrimidine-5-carboxylic acid (0.082 mmol) andN-Ethyl-N′-(3-dimethylaminopropyl) carbodiimide hydrochloride (0.087mmol). The reaction mixture was left with magnetic stirring for 2 hoursat which point water (1 mL) was added and the crude mixture was purifiedby HPLC to provide (R)-1-(2,5-difluoropyridin-3-yl)ethyl(1-methyl-4-(5-(2-(trifluoromethyl)pyrimidine-5-carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate(Compound 251). (MS (m/z) 550.0 [M+H]⁺). ¹H NMR (400 MHz, Methanol-d₄) δ9.47 (s, 2H), 8.95 (s, 1H), 8.25 (dd, J=8.6, 2.6 Hz, 1H), 8.03 (s, 1H),7.98 (dd, J=8.7, 0.7 Hz, 1H), 7.87 (s, 1H), 5.95 (d, J=7.1 Hz, 1H), 3.99(s, 3H), 1.61 (s, 3H).

Compounds 161-165 and 207-284 (Table 2) were similarly preparedaccording to Scheme C, Step 4 by reacting(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,Intermediate 5B (Example 22) with the Reagent listed in Table 2 in placeof 1-cyanocyclopropane-1-carboxylic acid following the general processdescribed for Compound 39.

To a mixture of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (Intermediate 5B) (0.073 mmol) in pyridine (0.5 mL) wasadded 3-cyanobicyclo[1.1.1]pentane-1-carboxylic acid (0.080 mmol) andN-Ethyl-N′-(3-dimethylaminopropyl) carbodiimide hydrochloride (0.080mmol). The reaction mixture was left with magnetic stirring for 2 hoursat which point water (1 mL) was added the crude mixture was purified byHPLC to provide (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(3-cyanobicyclo[1.1.1]pentane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 162). LCMS ((m/z) 495.175 [M+H]⁺). ¹H NMR (400 MHz,Methanol-d₄) δ 1H NMR (400 MHz, Methanol-d4) δ 8.83 (s, 1H), 8.22-7.58(m, 4H), 5.94 (d, J=7.0 Hz, 1H), 3.99 (s, 3H), 2.64 (s, 6H), 1.61 (s,3H).

Compounds 166-168, 285, and 288-290 (Table 2) were similarly preparedaccording to Scheme C, Step 4 by reacting(R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,Intermediate 5C (Example 23) with the Reagent listed in Table 2 in placeof 1-cyanocyclopropane-1-carboxylic acid following the general processdescribed for Compound 39.

To a mixture of (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (Intermediate 5C) (0.070 mmol) in pyridine (1.0 mL) wasadded 6-(trifluoromethyl)nicotinic acid (0.077 mmol) andN-Ethyl-N′-(3-dimethylaminopropyl) carbodiimide hydrochloride (0.084mmol). The reaction mixture was left with magnetic stirring for 2 hoursat which point water (1 mL) was added and the crude mixture was purifiedby HPLC to provide (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(1-methyl-4-(5-(6-(trifluoromethyl)nicotinamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate(Compound 288). (MS (m/z) 565.0 [M+H]⁺). ¹H NMR (400 MHz, Methanol-d₄) δ9.26 (d, J=2.1 Hz, 1H), 8.97 (s, 1H), 8.64-8.52 (m, 1H), 8.34-8.15 (m,2H), 8.11-7.68 (m, 3H), 6.03 (d, J=7.2 Hz, 1H), 4.00 (s, 3H), 1.60 (s,3H).

To a mixture of (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (Intermediate 5C) (0.054 mmol) in pyridine (2.0 mL) wasadded 1-(difluoromethyl)cyclopropane-1-carboxylic acid (0.081 mmol) andN-Ethyl-N′-(3-dimethylaminopropyl) carbodiimide hydrochloride (0.107mmol). The reaction mixture was left with magnetic stirring for 2 hours,concentrated and purified by HPLC to provide(R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-(1-(difluoromethyl)cyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 166). (MS (m/z) 510.15 [M+H]⁺). ¹H NMR (400 MHz, DMSO-d₆) δ9.86 (bs, 1H), 9.63 (s, 1H), 8.73 (s, 1H), 8.42 (bs, 1H), 8.10-7.82 (m,3H), 6.58 (t, J=56.9 Hz, 1H), 5.83 (bs, 1H), 3.89 (s, 3H), 1.57 (bs,3H), 1.43-1.27 (m, 2H), 1.24-1.03 (m, 2H).

Compounds 169-174 and 290-296 (Table 2) were similarly preparedaccording to Scheme C, Step 4 by reacting(R)-1-(2-fluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,Intermediate 5D (Example 24) with the Reagent listed in Table 2 in placeof 1-cyanocyclopropane-1-carboxylic acid following the general processdescribed for Compound 39.

Compounds 175-180 (Table 2) were similarly prepared according to SchemeC, Step 4 by reacting (R)-1-(5-fluoro-2-methylpyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,Intermediate 5E (Example 25) with the Reagent listed in Table 2 in placeof 1-cyanocyclopropane-1-carboxylic acid following the general processdescribed for Compound 39.

Compounds 181-182 (Table 2) were similarly prepared according to SchemeC, Step 4 by reacting 1-(2-chloro-6-fluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,Intermediate 5F (Example 34) with the Reagent listed in Table 2 in placeof 1-cyanocyclopropane-1-carboxylic acid following the general processdescribed for Compound 39.

Compounds 183-184 (Table 2) were similarly prepared according to SchemeC, Step 4 by reacting (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-amino-4-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,Intermediate 7B (Example 18) with the Reagent listed in Table 2 in placeof 1-cyanocyclopropane-1-carboxylic acid following the general processdescribed for Compound 39.

Compounds 201-204, 245-246, and 265-270 (Table 2) were prepared usingracemic mixtures of reagents listed in Table 2 and purified by chiralSFC purification to provide single stereoisomers.

TABLE 2 Compounds prepared according to Scheme C, Step 4. LCMS CompoundNo. Structure Reagent m/z 1H NMR Compound 39(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-(1-cyanocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

469.1 1H NMR (400 MHz, Methanol- d4) δ 8.79 (s, 1H), 8.33-7.46 (m, 4H),5.95 (d, J = 6.9 Hz, 1H), 4.00 (s, 3H), 1.82-1.36 (m, 7H). Compound 40(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(1-chlorocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

476.3 1H NMR (400 MHz, Methanol- d4) δ 8.87 (s, 1H), 8.48-7.76 (m, 4H),7.46 (s, 1H), 6.08 (q, J = 6.5 Hz, 1H), 3.99 (s, 3H), 1.76-1.70 (m, 2H),1.64 (d, J = 28.0 Hz, 3H), 1.46-1.38 (m, 2H). Compound 41(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(6,6-difluorospiro[3.3]heptane-2- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

532.2 1H NMR (400 MHz, Methanol- d4) δ 8.84 (s, 1H), 8.54-7.71 (m, 4H),7.46 (s, 1H), 6.07 (d, J = 7.1 Hz, 1H), 3.98 (s, 3H), 3.26 (p, J = 8.4Hz, 1H), 2.69 (td, J = 12.2, 2.6 Hz, 2H), 2.64-2.45 (m, 4H), 2.45- 2.31(m, 2H), 1.61 (s, 3H). Compound 42 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(2-oxaspiro[3.3]heptane-6- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

498.2 1H NMR (400 MHz, Methanol- d4) δ 8.83 (s, 1H), 8.52-7.74 (m, 4H),7.46 (s, 1H), 6.07 (d, J = 7.0 Hz, 1H), 4.76 (s, 2H), 4.70 (s, 2H), 3.98(s, 3H), 3.11 (p, J = 7.9 Hz, 1H), 2.56 (d, J = 8.0 Hz, 4H), 1.61 (s,3H). Compound 43 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(1,1-dioxidothietane-3- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

506.2 1H NMR (400 MHz, Methanol- d4) δ 8.84 (s, 1H), 8.48-7.73 (m, 4H),7.47 (s, 1H), 6.07 (d, J = 7.2 Hz, 1H), 4.63-4.45 (m, 2H), 4.45- 4.25(m, 2H), 3.55 (tt, J = 9.8, 7.6 Hz, 1H), 1.61 (s, 3H). Compound 44(R)-1-(2-chloropyridin-3-yl)ethyl (1- methyl-4-(5-(3-(oxetan-3-yl)bicyclo[1.1.1]pentane-1- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

524.2 1H NMR (400 MHz, Methanol- d4) δ 8.92 (s, 1H), 8.46-7.70 (m, 4H),7.47 (s, 1H), 6.08 (d, J = 7.1 Hz, 1H), 4.81 (dd, J = 7.9, 6.0 Hz, 2H),4.52 (t, J = 6.0 Hz, 2H), 3.99 (s, 3H), 3.18 (tt, J = 8.0, 5.9 Hz, 1H),2.15 (s, 6H), 1.61 (s, 3H). Compound 45(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(3-(difluoromethyl)bicyclo[1.1.1]pentane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

518.2 1H NMR (400 MHz, Methanol- d4) δ 8.91 (s, 1H), 8.53-7.79 (m, 4H),7.46 (s, 1H), 6.25-5.60 (m, 2H), 3.99 (s, 3H), 2.26 (s, 6H), 1.61 (s,3H). Compound 46 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(3-methoxybicyclo[1.1.1]pentane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

498.1 1H NMR (400 MHz, Methanol- d4) δ 8.90 (s, 1H), 8.47-7.76 (m, 4H),7.46 (s, 1H), 6.08 (d, J = 6.9 Hz, 1H), 3.99 (s, 3H), 3.36 (s, 3H), 2.28(s, 6H), 1.61 (s, 3H). Compound 47 (R)-1-(2-chloropyridin-3-yl)ethyl (1-methyl-4-(5-(3- methylbicyclo[1.1.1]pentane-1-carboxamido)pyridin-2-yl)-1H-1,2,3- triazol-5-yl)carbamate

482.2 1H NMR (400 MHz, Methanol- d4) δ 8.90 (s, 1H), 8.48-7.71 (m, 4H),7.46 (s, 1H), 6.08 (d, J = 7.0 Hz, 1H), 3.98 (s, 3H), 2.05 (s, 6H), 1.61(s, 3H), 1.26 (s, 3H). Compound 48 (R)-1-(2-chloropyridin-3-yl)ethyl (1-methyl-4-(5-(1- (trifluoromethyl)cyclobutane-1-carboxamido)pyridin-2-yl)-1H-1,2,3- triazol-5-yl)carbamate

524.2 1H NMR (400 MHz, Methanol- d4) δ 8.90 (s, 1H), 8.46-7.74 (m, 4H),7.46 (s, 1H), 6.08 (d, J = 6.7 Hz, 1H), 3.99 (s, 3H), 2.90-2.69 (m, 2H),2.60 (ddt, J = 9.5, 7.7, 5.7 Hz, 2H), 2.20-1.96 (m, 2H), 1.61 (s, 3H).Compound 49 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(2,2-dimethylcyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

470.2 1H NMR (400 MHz, Methanol- d4) δ 8.85 (s, 1H), 8.43-7.68 (m, 4H),7.46 (s, 1H), 6.08 (d, J = 6.5 Hz, 1H), 3.98 (s, 3H), 1.82-1.43 (m, 4H),1.30-1.21 (m, 6H), 1.21- 1.16 (m, 1H), 0.90 (dd, J = 7.9, 4.3 Hz, 1H).Compound 50 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((1S,2S)-2-cyanocyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

467.0 1H NMR (400 MHz, Methanol- d4) δ 8.84 (s, 1H), 8.55-7.00 (m, 5H),6.08 (d, J = 7.1 Hz, 1H), 3.99 (s, 3H), 2.48 (ddd, J = 8.6, 5.9, 4.2 Hz,1H), 2.23-2.03 (m, 1H), 1.58 (dddd, J = 14.8, 8.6, 6.0, 4.6 Hz, 5H).Compound 51 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((1R,2R)-2-cyanocyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

467.0 1H NMR (400 MHz, Methanol- d4) δ 8.84 (s, 1H), 8.52-7.18 (m, 5H),6.08 (d, J = 6.8 Hz, 1H), 3.99 (s, 3H), 2.48 (ddd, J = 8.6, 5.9, 4.3 Hz,1H), 2.24-2.02 (m, 1H), 1.59 (dddd, J = 16.1, 8.5, 6.0, 4.6 Hz, 5H).Compound 52 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((1R,2S)-2-fluorocyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

460.1 1H NMR (400 MHz, Methanol- d4) δ 8.82 (s, 1H), 8.48-7.73 (m, 4H),7.46 (s, 1H), 6.08 (d, J = 6.7 Hz, 1H), 4.96 (ddd, J = 6.2, 3.3, 1.6 Hz,1H), 2.29 (dddd, J = 17.3, 10.5, 6.6, 1.6 Hz, 1H), 1.91-1.15 (m, 5H).Compound 53 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((1S,2S)-2-fluorocyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

460.2 1H NMR (400 MHz, Methanol- d4) δ 8.86 (s, 1H), 8.61-7.72 (m, 4H),7.47 (s, 1H), 6.08 (d, J = 6.7 Hz, 1H), 4.97 (td, J = 6.2, 3.7 Hz, 1H),3.99 (s, 3H), 2.09-2.01 (m, 1H), 1.82 (dtd, J = 23.0, 7.1, 3.7 Hz, 1H),1.61 (s, 3H), 1.23 (dddd, J = 12.7, 9.2, 7.0, 6.0 Hz, 1H). Compound 54(R)-1-(2-chloropyridin-3-yl)ethyl (1- methyl-4-(5-(oxetane-2-carboxamido)pyridin-2-yl)-1H-1,2,3- triazol-5-yl)carbamate

458.2 1H NMR (400 MHz, Methanol- d4) δ 8.96 (s, 1H), 8.48-7.77 (m, 4H),7.47 (s, 1H), 6.08 (d, J = 6.5 Hz, 1H), 5.21 (ddd, J = 9.2, 6.7, 0.8 Hz,1H), 4.86-4.73 (m, 2H), 3.99 (s, 3H), 3.14 (dtd, J = 11.5, 8.9, 6.5 Hz,1H), 2.79 (ddtd, J = 11.4, 9.2, 6.9, 2.6 Hz, 1H), 1.61 (s, 3H). Compound55 (R)-1-(2-chloropyridin-3-yl)ethyl (1- methyl-4-(5-(1-(trifluoromethyl)cyclopropane-1- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

510.2 1H NMR (400 MHz, Methanol- d4) δ 8.84 (s, 1H), 8.58-7.72 (m, 4H),7.46 (s, 1H), 6.08 (d, J = 6.8 Hz, 1H), 3.99 (s, 3H), 1.92-1.16 (m, 7H).Compound 56 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((1R,2R)-2-fluorocyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

460.1 1H NMR (400 MHz, Methanol- d4) δ 8.87 (s, 1H), 8.51-7.71 (m, 4H),7.46 (s, 1H), 6.08 (q, J = 6.6 Hz, 1H), 4.98 (td, J = 6.2, 3.7 Hz, 1H),3.99 (s, 3H), 2.11-2.01 (m, 1H), 1.82 (dtd, J = 23.0, 7.1, 3.7 Hz, 1H),1.62 (s, 3H), 1.23 (dddd, J = 12.8, 9.3, 7.0, 6.0 Hz, 1H). Compound 57(R)-1-(2-chloropyridin-3-yl)ethyl (1- methyl-4-(5-(oxetane-3-carboxamido)pyridin-2-yl)-1H-1,2,3- triazol-5-yl)carbamate

458.2 1H NMR (400 MHz, Methanol- d4) δ 8.86 (s, 1H), 8.53-7.77 (m, 4H),7.47 (s, 1H), 6.07 (s, 1H), 4.92 (q, J = 6.2, 4.3 Hz, 4H), 4.02 (d, J =30.2 Hz, 4H), 1.58 (d, J = 28.0 Hz, 3H). Compound 58(R)-1-(2-chloropyridin-3-yl)ethyl (1-methyl-4-(5-(nicotinamido)pyridin-2- yl)-1H-1,2,3-triazol-5-yl)carbamate

479.2 1H NMR (400 MHz, Methanol- d4) δ 9.16 (dd, J = 2.3, 0.9 Hz, 1H),9.02 (s, 1H), 8.77 (dd, J = 4.9, 1.6 Hz, 1H), 8.42 (ddd, J = 8.0, 2.3,1.6 Hz, 1H), 8.32 (s, 1H), 8.25-7.83 (m, 3H), 7.64 (ddd, J = 8.0, 4.9,0.9 Hz, 1H), 7.49 (s, 1H), 6.09 (d, J = 6.8 Hz, 1H), 4.00 (s, 3H), 1.62(s, 3H). Compound 59 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(2-cyanoacetamido)pyridin-2-yl)-1- methyl-1H-1,2,3-triazol-5-yl)carbamate

441.1 1H NMR (400 MHz, Methanol- d4) δ 8.82 (s, 1H), 8.52-7.74 (m, 4H),7.44 (dd, J = 7.8, 4.8 Hz, 1H), 6.08 (d, J = 6.9 Hz, 1H), 3.99 (s, 3H),3.84 (s, 2H), 1.95-1.09 (m, 3H). Compound 60(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(1-fluorocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

460.1 1H NMR (400 MHz, Methanol- d4) δ 8.93 (s, 1H), 8.57-7.74 (m, 4H),7.47 (s, 1H), 6.08 (q, J = 6.6 Hz, 1H), 3.99 (s, 3H), 1.84-1.34 (m, 7H).Compound 61 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(isonicotinamido)pyridin-2-yl)-1- methyl-1H-1,2,3-triazol-5-yl)carbamate

479.1 1H NMR (400 MHz, Methanol- d4) δ 9.02 (s, 1H), 8.87-8.70 (m, 2H),8.48-7.77 (m, 6H), 7.49 (s, 1H), 6.09 (d, J = 6.7 Hz, 1H), 4.00 (s, 3H),1.62 (s, 3H). Compound 62 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((1r,3R)-3-fluorocyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

474.2 1H NMR (400 MHz, Methanol- d4) δ 8.84 (s, 1H), 8.50-7.77 (m, 4H),6.08 (d, J = 6.2 Hz, 1H), 5.48- 5.07 (m, 1H), 3.99 (s, 3H), 2.78- 2.38(m, 4H), 1.61 (s, 3H). Compound 63 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(2,2-difluorocyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

492.1 1H NMR (400 MHz, Methanol- d4) δ 8.88 (s, 1H), 8.57-7.73 (m, 4H),7.47 (s, 1H), 6.08 (q, J = 6.5 Hz, 1H), 3.99 (s, 3H), 3.93-3.77 (m, 1H),2.64 (dddd, J = 13.4, 11.8, 9.3, 7.6 Hz, 2H), 2.33 (tt, J = 12.0, 7.6Hz, 1H), 2.11-2.00 (m, 1H), 1.61 (s, 3H). Compound 64(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(3-cyanobicyclo[1.1.1]pentane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

493.2 1H NMR (400 MHz, Methanol- d4) δ 8.88 (s, 1H), 8.51-7.74 (m, 4H),7.46 (s, 1H), 6.07 (d, J = 6.4 Hz, 1H), 3.98 (s, 3H), 2.64 (s, 6H), 1.61(s, 3H). Compound 65 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((S)-2,2-difluorocyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

478.1 1H NMR (400 MHz, Methanol- d4) δ 8.85 (s, 1H), 8.53-7.74 (m, 4H),7.47 (s, 1H), 6.08 (d, J = 7.0 Hz, 1H), 2.76 (ddd, J = 13.1, 10.8, 7.7Hz, 1H), 2.16 (dtd, J = 12.7, 7.7, 6.1 Hz, 1H), 1.90 (dddd, J = 12.6,10.8, 7.8, 4.9 Hz, 1H), 1.61 (s, 3H). Compound 66(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(1-cyanocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

481.2 1H NMR (400 MHz, Methanol- d4) δ 8.88 (s, 1H), 8.46-7.75 (m, 4H),7.47 (s, 1H), 6.08 (d, J = 6.9 Hz, 1H), 3.99 (s, 3H), 2.89 (dtd, J =11.0, 7.4, 1.5 Hz, 2H), 2.76- 2.64 (m, 2H), 2.30 (dtt, J = 11.6, 9.2,7.4 Hz, 1H), 2.21-2.02 (m, 1H), 1.61 (s, 3H). Compound 67(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(1-cyanocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

467.1 1H NMR (400 MHz, Methanol- d4) δ 8.84 (s, 1H), 8.50-7.76 (m, 4H),7.46 (s, 1H), 6.30-5.74 (m, 1H), 3.99 (s, 3H), 1.84-1.38 (m, 7H).Compound 68 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(bicyclo[1.1.1]pentane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

468.2 1H NMR (400 MHz, Methanol- d4) δ 8.90 (s, 1H), 8.47-7.71 (m, 4H),7.46 (s, 1H), 6.08 (d, J = 6.8 Hz, 1H), 3.98 (s, 3H), 2.53 (s, 1H), 2.22(s, 6H), 1.61 (s, 3H). Compound 69 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((1S,2R)-2-fluorocyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

460.2 1H NMR (400 MHz, Methanol- d4) δ 8.82 (s, 1H), 8.48-7.71 (m, 4H),7.46 (s, 1H), 6.08 (d, J = 6.7 Hz, 1H), 4.96 (ddd, J = 6.2, 3.4, 1.6 Hz,1H), 3.98 (s, 3H), 2.29 (dddd, J = 17.3, 10.4, 6.6, 1.6 Hz, 1H),1.89-1.16 (m, 5H). Compound 70 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(3-fluorobicyclo[1.1.1]pentane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

486.2 1H NMR (400 MHz, Methanol- d4) δ 8.89 (s, 1H), 8.47-7.71 (m, 4H),7.46 (s, 1H), 6.08 (d, J = 6.9 Hz, 1H), 3.99 (s, 3H), 2.47 (d, J = 2.4Hz, 6H), 1.61 (s, 3H). Compound 71 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((1s,3S)-3-fluorocyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

474.2 1H NMR (400 MHz, Methanol- d4) δ 8.86 (s, 1H), 8.54-7.79 (m, 4H),7.47 (s, 1H), 6.08 (d, J = 7.0 Hz, 1H), 5.12-4.89 (m, 1H), 2.84- 2.71(m, 1H), 2.71-2.58 (m, 2H), 2.50 (ddddd, J = 19.4, 11.9, 9.6, 7.6, 2.0Hz, 2H), 1.61 (s, 3H). Compound 72 (R)-1-(2-chloroypridin-3-yl)ethyl (1-methyl-4-(5-(3- (trifluoromethyl)bicyclo[1.1.1]pentane-1-carboxamido)pyridin-2-yl)-1H-1,2,3- triazol-5-yl)carbamate

536.2 1H NMR (400 MHz, Methanol- d4) δ 8.90 (s, 1H), 8.44-7.71 (m, 4H),7.46 (s, 1H), 6.08 (d, J = 6.5 Hz, 1H), 3.99 (s, 3H), 2.39 (s, 6H), 1.61(s, 3H). Compound 73 (R)-1-(2-chloropyridin-3-yl)ethyl (1-methyl-4-(5-(spiro[3.3]heptane-2- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

496.2 1H NMR (400 MHz, Methanol- d4) δ 8.84 (s, 1H), 8.46-7.69 (m, 4H),7.47 (s, 1H), 6.07 (d, J = 6.9 Hz, 1H), 3.98 (s, 3H), 3.16 (p, J = 8.5Hz, 1H), 2.39-2.20 (m, 4H), 2.14 (ddd, J = 7.3, 5.9, 1.2 Hz, 2H), 1.99(dd, J = 8.5, 5.9 Hz, 2H), 1.92-1.79 (m, 2H), 1.61 (s, 3H). Compound 74(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(1-cyanospiro[2.3]hexane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

507.2 1H NMR (400 MHz, Methanol- d4) δ 8.85 (s, 1H), 8.52-7.73 (m, 4H),7.46 (s, 1H), 6.25-5.91 (m, 1H), 3.99 (s, 3H), 2.65 (ddd, J = 12.0, 9.3,6.8 Hz, 1H), 2.40-2.06 (m, 6H), 1.90-1.36 (m, 4H). Compound 75(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(3-cyclopropylpropiolamido)pyridin-2- yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

466.2 1H NMR (400 MHz, Methanol- d4) δ 8.83 (s, 1H), 8.49-7.69 (m, 4H),7.46 (s, 1H), 6.07 (d, J = 6.7 Hz, 1H), 3.98 (s, 3H), 1.91-1.33 (m, 4H),1.07-1.00 (m, 2H), 0.95- 0.86 (m, 2H). Compound 76(R)-1-(2-chloropyridin-3-yl)ethyl (4 (5-(but-2-ynamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5- yl)carbamate

440.0 1H NMR (400 MHz, Methanol- d4) δ 8.84 (s, 1H), 8.48-7.75 (m, 4H),7.46 (s, 1H), 6.08 (d, J = 6.7 Hz, 1H), 3.98 (s, 3H), 2.08 (s, 3H), 1.61(s, 3H). Compound 77 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(dispiro[3.1.36.14]decane-2- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

537.2 1H NMR (400 MHz, Methanol- d4) δ 8.83 (s, 1H), 8.52-7.70 (m, 4H),7.46 (s, 1H), 6.07 (d, J = 7.0 Hz, 1H), 3.98 (s, 3H), 3.19 (q, J = 8.5Hz, 1H), 2.34 (td, J = 10.0, 1.7 Hz, 2H), 2.21 (dd, J = 11.9, 8.6 Hz,2H), 2.15 (s, 2H), 2.03-1.92 (m, 6H), 1.89-1.77 (m, 2H), 1.61 (s, 3H).Compound 78 (R)-1-(2-chloropyridin-3-yl)ethyl (1- methyl-4-(5-(2-(trifluoromethyl)spiro[3.3]heptane-2-carboxamido)pyridin-2-yl)-1H-1,2,3- triazol-5-yl)carbamate

564.1 1H NMR (400 MHz, Methanol- d4) δ 8.88 (s, 1H), 8.53-7.74 (m, 4H),7.46 (s, 1H), 6.08 (d, J = 6.8 Hz, 1H), 3.99 (s, 3H), 2.77 (d, J = 13.3Hz, 2H), 2.62 (d, J = 13.8 Hz, 2H), 2.10 (dt, J = 21.0, 7.5 Hz, 4H),1.92-1.81 (m, 2H), 1.61 (s, 3H). Compound 79(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(2-cyanospiro[3.3]heptane-2-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

521.2 1H NMR (400 MHz, Methanol- d4) δ 8.86 (s, 1H), 8.46-7.74 (m, 4H),7.47 (s, 1H), 6.08 (d, J = 6.8 Hz, 1H), 3.99 (s, 3H), 2.96-2.80 (m, 2H),2.80-2.58 (m, 2H), 2.28 (t, J = 7.5 Hz, 2H), 2.07 (dd, J = 8.7, 6.1 Hz,2H), 1.97-1.85 (m, 2H), 1.61 (s, 3H). Compound 80(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(6-cyanospiro[3.3]heptane-2-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

521.3 1H NMR (400 MHz, Methanol- d4) δ 8.83 (s, 1H), 8.49-7.74 (m, 4H),7.46 (s, 1H), 6.07 (d, J = 7.0 Hz, 1H), 3.98 (s, 3H), 3.18 (h, J = 8.2Hz, 2H), 2.60 (ddd, J = 11.6, 8.4, 3.3 Hz, 1H), 2.42 (dddd, J = 29.1,15.3, 11.7, 7.0 Hz, 7H), 1.61 (s, 3H). Compound 81(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(6-fluorospiro[3.3]heptane-2-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

514.3 1H NMR (400 MHz, Methanol- d4) δ 8.84 (s, 1H), 8.58-7.71 (m, 4H),7.47 (s, 1H), 6.07 (d, J = 6.8 Hz, 1H), 5.00 (p, J = 6.7 Hz, 1H), 3.98(s, 3H), 3.24 (p, J = 8.4 Hz, 1H), 2.60 (dq, J = 12.5, 6.4 Hz, 1H),2.53-2.34 (m, 3H), 2.34- 2.08 (m, 4H), 1.61 (s, 3H). Compound 82(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(3-chlorobicyclo[1.1.1]pentane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

502.2 1H NMR (400 MHz, Methanol- d4) δ 8.88 (s, 1H), 8.52-7.72 (m, 4H),7.46 (s, 1H), 6.07 (d, J = 7.0 Hz, 1H), 3.98 (s, 3H), 2.54 (s, 6H), 1.61(s, 3H). Compound 83 (R)-1-(2-chloropyridin-3-yl)ethyl (1-methyl-4-(5-(3-oxocyclobutane-1- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

470.2 1H NMR (400 MHz, Methanol- d4) δ 8.88 (s, 1H), 8.54-7.72 (m, 4H),7.47 (s, 1H), 6.08 (d, J = 7.0 Hz, 1H), 3.99 (s, 3H), 3.57-3.34 (m, 5H),1.61 (s, 3H). Compound 84 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(3,3-dimethylcyclobutane-l- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

484.2 1H NMR (400 MHz, Methanol- d4) δ 8.85 (s, 1H), 8.55-7.77 (m, 4H),7.47 (s, 1H), 6.08 (d, J = 6.7 Hz, 1H), 3.98 (s, 3H), 3.25 (q, J = 8.7Hz, 1H), 2.17 (ddd, J = 10.8, 9.2, 1.9 Hz, 2H), 2.09-1.96 (m, 2H), 1.61(s, 3H), 1.26 (s, 3H), 1.16 (s, 3H). Compound 85(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-((3R,5r)-1,1-difluorospiro[2.3]hexane-5- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

518.1 1H NMR (400 MHz, Methanol- d4) δ 8.87 (s, 1H), 8.46-7.72 (m, 4H),7.48 (s, 1H), 6.08 (d, J = 6.7 Hz, 1H), 3.99 (s, 3H), 3.55-3.41 (m, 1H),2.71 (dd, J = 12.5, 6.6 Hz, 2H), 2.39 (t, J = 11.1 Hz, 2H), 1.61 (s,3H), 1.36 (t, J = 8.5 Hz, 2H). Compound 86(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-((3S,5s)-1,1-difluorospiro[2.3]hexane-5- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

518.7 1H NMR (400 MHz, Methanol- d4) δ 8.86 (s, 1H), 8.53-7.73 (m, 4H),7.47 (s, 1H), 6.08 (d, J = 7.5 Hz, 1H), 3.99 (s, 3H), 3.41 (t, J = 8.7Hz, 1H), 2.66-2.46 (m, 4H), 1.61 (s, 3H), 1.30 (t, J = 8.5 Hz, 2H).Compound 87 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(5-cyanospiro[2.3]hexane-5- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

507.2 1H NMR (400 MHz, Methanol- d4) δ 8.89 (s, 1H), 8.55-7.72 (m, 4H),7.47 (s, 1H), 6.31-5.75 (m, 1H), 3.99 (s, 3H), 3.05 (dd, J = 11.7, 1.7Hz, 2H), 2.77 (dt, J = 11.1, 1.6 Hz, 2H), 1.62 (s, 3H), 0.78-0.64 (m,2H), 0.64-0.47 (m, 2H). Compound 88 (R)-1-(2-chloropyridin-3-yl)ethyl(1- methyl-4-(5-(spiro[2.3]hexane-5- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

482.3 1H NMR (400 MHz, Methanol- d4) δ 8.87 (s, 1H), 8.54-7.74 (m, 4H),7.47 (s, 1H), 6.08 (d, J = 6.7 Hz, 1H), 3.99 (s, 3H), 3.48 (tt, J = 8.9,7.6 Hz, 1H), 2.69-2.54 (m, 2H), 2.36-2.20 (m, 2H), 1.61 (s, 3H),0.64-0.31 (m, 4H). Compound 89 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(1-cyanospiro[2.4]heptane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

521.2 1H NMR (400 MHz, Methanol- d4) δ 8.85 (s, 1H), 8.47-7.70 (m, 4H),7.47 (s, 1H), 6.08 (d, J = 6.9 Hz, 1H), 3.99 (s, 3H), 2.26-2.07 (m, 2H),1.95-1.44 (m, 11H). Compound 90 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((S)-2,2-difluorocyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

492.1 1H NMR (400 MHz, Acetonitrile- d3) δ 7.50 (s, 1H), 7.05-6.42 (m,4H), 6.09 (s, 1H), 4.71 (d, J = 6.9 Hz, 1H), 2.56-2.37 (m, 1H), 1.36-1.15 (m, 2H), 0.95 (d, J = 11.4 Hz, 1H), 0.65 (s, 1H), 0.24 (s, 3H).Compound 91 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((R)-2,2-difluorocyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

492.0 1H NMR (400 MHz, Methanol- d4) δ 8.85 (s, 1H), 8.40-7.77 (m, 4H),7.44 (s, 1H), 6.06 (d, J = 6.9 Hz, 1H), 3.97 (s, 3H), 3.92-3.72 (m, 1H),2.71-2.50 (m, 2H), 2.30 (d, J = 11.4 Hz, 1H), 2.00 (s, 1H), 1.59 (s,3H). Compound 92 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(1-carbamoylcyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

485.1 1H NMR (400 MHz, Acetonitrile- d3) δ 11.63 (s, 1H), 8.99 (d, J =2.5 Hz, 1H), 8.57 (s, 1H), 8.34 (dd, J = 4.8, 1.9 Hz, 1H), 8.23 (dd, J =8.8, 2.5 Hz, 1H), 8.03 (d, J = 8.8 Hz, 1H), 7.92 (s, 1H), 7.40 (d, J =6.6 Hz, 1H), 6.33 (s, 1H), 6.04 (q, J = 6.6 Hz, 2H), 3.96 (s, 3H), 1.70(q, J = 4.4 Hz, 2H), 1.58 (d, J = 6.5 Hz, 3H), 1.52 (q, J = 4.4 Hz, 2H).Compound 93 (R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(3-cyanooxetane-3-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

483.1 1H NMR (400 MHz, DMSO-d6) δ 10.82 (s, 1H), 9.95 (s, 1H), 8.78 (s,1H), 8.36 (s, 1H), 8.07 (dd, J = 8.6, 2.6 Hz, 1H), 8.02-7.90 (m, 2H),7.61-7.45 (m, 1H), 5.89 (d, J = 7.1 Hz, 1H), 5.09-4.93 (m, 4H), 3.89 (s,3H), 1.53 (s, 3H). Compound 94 (R)-1-(2-chloropyridin-3-yl)ethyl (1-methyl-4-(5-(1-(pyridin-3- yl)cyclopropane-1-carboxamido)pyridin-2-yl)-1H-1,2,3- triazol-5-yl)carbamate

519.1 1H NMR (400 MHz, DMSO-d6) δ 9.81 (brs, 1H), 9.43 (s, 1H), 8.72 (s,1H), 8.65 (d, J = 2.3 Hz, 1H), 8.53 (dd, J = 4.8, 1.6 Hz, 1H), 8.35 (s,1H), 7.99 (dd, J = 8.7, 2.6 Hz, 1H), 7.92-7.75 (m, 2H), 7.50- 7.40 (m,3H), 5.86 (m, 1H), 3.87 (s, 3H), 1.61-1.57 (m, 4H), 1.25- 1.24 (m, 3H).Compound 95 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(4-cyanotetrahydro-2H-pyran-4- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

511.2 1H NMR (400 MHz, DMSO-d6) δ 10.42 (s, 1H), 9.85 (brs,1H), 8.80 (s,1H), 8.36 (s, 1H), 8.08 (dd, J = 8.6, 2.5 Hz, 1H), 7.94 (d, J = 8.6 Hz,2H), 7.60-7.45 (m, 1H), 5.95- 5.83 (m, 1H), 4.00 (dt, J = 12.2, 3.4 Hz,2H), 3.88 (s, 3H), 3.60 (ddd, J = 12.4, 9.9, 3.8 Hz, 2H), 2.26-2.09 (m,4H), 1.65-1.40 (m, 3H) Compound 96 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(3-ethyloxetane-3- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

486.2 1H NMR (400 MHz, DMSO-d6) δ 9.98 (s, 1H), 9.73 (s, 1H), 8.85- 8.78(m, 1H), 8.40-8.32 (m, 1H), 8.07 (dd, J = 8.6, 2.5 Hz, 1H), 7.91 (d, J =8.6 Hz, 1H), 7.62-7.45 (m, 2H), 5.92-5.80 (m, 1H), 4.84 (d, J = 6.2 Hz,2H), 4.42 (d, J = 6.2 Hz, 2H), 3.88 (s, 3H), 2.10 (q, J = 7.4 Hz, 2H),1.75-1.45 (m, 3H), 0.87 (t, J = 7.4 Hz, 3H). Compound 97(R)-1-(2-chloropyridin-3-yl)ethyl (1- methyl-4-(5-(3-methyloxetane-3-carboxamido)pyridin-2-yl)-1H-1,2,3- triazol-5-yl)carbamate

472.2 1H NMR (400 MHz, DMSO-d6) δ 10.01 (s, 1H), 9.85 (s, 1H), 8.81 (s,1H), 8.45-8.35 (m, 1H), 8.08 (dd, J = 8.6, 2.5 Hz, 1H), 7.92 (d, J = 8.6Hz, 1H), 7.65-7.43 (m, 2H), 5.95-5.82 (m, 1H), 4.88 (d, J = 6.0 Hz, 2H),4.39 (d, J = 6.1 Hz, 2H), 3.89 (s, 3H), 1.65 (s, 3H), 1.55 (s, 3H)Compound 98 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(6-cyanopicolinamido)pyridin-2-yl)- 1-methyl-1H-1,2,3-triazol-5-yl)carbamate

504.1 ¹H NMR (400 MHz, Methanol-d₄) δ 9.11 (s, 1H), 8.51 (d, J = 7.7 Hz,1H), 8.38-8.22 (m, 4H), 8.16- 8.08 (m, 2H), 7.98 (d, J = 8.7 Hz, 1H),6.07 (s, 1H), 3.98 (s, 3H), 1.61 (s, 3H). Compound 99(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(6-cyanonicotinamido)pyridin-2-yl)- 1-methyl-1H-1,2,3-triazol-5-yl)carbamate

504.2 ¹H NMR (400 MHz, Methanol-d₄) δ 9.25 (dd, J = 2.2, 0.8 Hz, 1H),9.00 (s, 1H), 8.52 (dd, J = 8.1, 2.2 Hz, 1H), 8.30 (s, 1H), 8.21 (dd, J= 8.6, 2.6 Hz, 1H), 8.06 (dd, J = 8.1, 0.9 Hz, 1H), 8.00-7.37 (m, 3H),6.07 (d, J = 6.9 Hz, 1H), 3.98 (s, 3H), 1.60 (s, 3H). Compound 100(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(2-cyanoisonicotinamido)pyridin-2- yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

504.2 ¹H NMR (400 MHz, Methanol-d₄) δ 9.00 (s, 1H), 8.93 (dd, J = 5.1,0.9 Hz, 1H), 8.40 (dd, J = 1.7, 0.9 Hz, 1H), 8.30 (s, 1H), 8.21 (dd, J =8.6, 2.6 Hz, 1H), 8.18-8.04 (m, 2H), 7.97 (d, J = 8.6 Hz, 1H), 7.56-7.39 (m, 1H), 6.07 (s, 1H), 3.98 (s, 3H), 1.60 (s, 3H). Compound 101(R)-1-(2-chloropyridin-3-yl)ethyl (1- methyl-4-(5-(3-methylisonicotinamido)pyridin-2-yl)- 1H-1,2,3-triazol-5-yl)carbamate

493.0 1H NMR (400 MHz, Methanol- d4) δ 8.94 (s, 1H), 8.56 (s, 1H), 8.54(d, J = 5.0 Hz, 1H), 8.30 (s, 1H), 8.16 (dd, J = 8.6, 2.6 Hz, 1H), 8.06(s, 1H), 7.95 (d, J = 8.6 Hz, 1H), 7.56 (d, J = 5.0 Hz, 1H), 7.47 (s,1H), 6.07 (d, J = 6.2 Hz, 1H), 3.98 (s, 3H), 2.50 (s, 3H), 1.60 (s, 3H).Compound 102 (R)-1-(2-chloropyridin-3-yl)ethyl (1- methyl-4-(5-(2-methylisonicotinamido)pyridin-2-yl)- 1H-1,2,3-triazol-5-yl)carbamate

493.0 1H NMR (400 MHz, Methanol- d4) δ 9.00 (s, 1H), 8.62 (d, J = 5.2Hz, 1H), 8.30 (s, 1H), 8.20 (dd, J = 8.7, 2.6 Hz, 1H), 8.07 (s, 1H),7.96 (d, J = 8.7 Hz, 1H), 7.82 (s, 1H), 7.73 (dd, J = 5.3, 1.6 Hz, 1H),7.47 (s, 1H), 6.07 (d, J = 6.8 Hz, 1H), 3.98 (s, 3H), 2.66 (s, 3H), 1.60(s, 3H). Compound 103 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(2-chloroisonicotinamido)pyridin-2- yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

513.2 1H NMR (400 MHz, Methanol- d4) δ 9.00 (s, 1H), 8.59 (dd, J = 5.1,0.7 Hz, 1H), 8.30 (s, 1H), 8.20 (dd, J = 8.7, 2.6 Hz, 1H), 8.07 (s, 1H),8.03-7.90 (m, 2H), 7.87 (dd, J = 5.1, 1.5 Hz, 1H), 7.47 (s, 1H), 6.07(d, J = 6.8 Hz, 1H), 3.98 (s, 3H), 1.60 (s, 3H). Compound 104(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(2-oxabicyclo[2.1.1]hexane-4-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

484.1 1H NMR (400 MHz, DMSO-d6) δ 10.04-9.54 (m, 2H), 8.86 (bs, 1H),8.36 (bs, 1H), 8.20-7.83 (m, 3H), 7.53 (bs, 1H), 5.88 (bs, 1H), 4.52 (s,1H), 3.98-3.75 (m, 5H), 2.28- 2.15 (m, 2H), 1.87-1.74 (m, 2H), 1.56 (bs,3H). Compound 105 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(2-oxabicyclo[2.1.1]hexane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

484.2 1H NMR (400 MHz, DMSO-d6) δ 10.09 (s, 1H), 9.85 (bs, 1H), 8.93(bs, 1H), 8.36 (bs, 1H), 8.21 (dd, J = 8.6, 2.5 Hz, 1H), 8.04 (bs, 1H),7.90 (d, J = 8.7 Hz, 1H), 7.55 (bs, 1H), 5.87 (bs, 1H), 3.99-3.75 (m,5H), 3.00 (t, J = 3.3 Hz, 1H), 2.27- 2.11 (m, 2H), 1.77-1.30 (m, 5H).Compound 106 (R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(1H-imidazole-4-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

482.1 1H NMR (400 MHz, DMSO-d6) δ 10.29 (s, 1H), 9.83 (bs, 1H), 8.88 (s,1H), 8.36 (bs, 1H), 8.16 (dd, J = 8.6, 2.6 Hz, 1H), 8.09-7.73 (m, 4H),7.52 (bs, 1H), 5.87 (bs, 1H), 3.97-3.80 (m, 6H), 1.51 (bs, 3H). Compound107 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(3,3-difluoropropanamido)pyridin- 2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

468.2 ¹H NMR (400 MHz, DMSO-d₆) δ 12.70 (s, 1H), 10.24 (s, 1H), 9.83(bs, 1H), 9.06 (s, 1H), 8.48-8.25 (m, 2H), 8.06 (bs, 1H), 7.96-7.78 (m,3H), 7.60 (bs, 1H), 5.88 (bs, 1H), 3.88 (s, 3H), 1.57 (bs, 3H). Compound108 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(3-hydroxy-3-methylcyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

466.1 1H NMR (400 MHz, DMSO-d6) δ 10.48 (s, 1H), 9.82 (bs, 1H), 8.75(bs, 1H), 8.36 (bs, 1H), 8.04 (dd, J = 8.6, 2.5 Hz, 1H), 7.93 (d, J =8.6 Hz, 1H), 7.53 (bs, 2H), 6.42 (tt, J = 55.8, 4.8 Hz, 1H), 5.87 (bs,1H), 3.88 (s, 3H), 3.13 (td, J = 16.8, 4.8 Hz, 2H), 1.56 (bs, 3H).Compound 109 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(3-hydroxy-3-methylcyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

486.1 1H NMR (400 MHz, DMSO-d6) δ 10.09 (s, 1H), 9.83 (bs, 1H), 8.77(bs, 1H), 8.36 (bs, 1H), 8.10-7.99 (m, 2H), 7.88 (d, J = 8.6 Hz, 1H),7.53 (bs, 1H), 5.87 (bs, 1H), 5.10 (s, 1H), 3.87 (s, 3H), 2.80-2.71 (m,1H), 2.32-2.17 (m, 2H), 2.15-2.10 (m, 2H), 1.55 (bs, 3H), 1.29 (s, 3H).Compound 110 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(1-(fluoromethyl)cyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

474.2 1H NMR (400 MHz, DMSO-d6) δ 9.83 (bs, 1H), 9.62 (s, 1H), 8.81 (bs,1H), 8.36 (bs, 1H), 8.08 (dd, J = 8.6, 2.5 Hz, 2H), 7.90 (d, J = 8.6 Hz,1H), 7.53 (bs, 1H), 5.87 (bs, 1H), 4.71 (d, J = 48.5 Hz, 2H), 3.87 (s,3H), 1.56 (bs, 3H), 1.40- 1.27 (m, 2H), 1.01 (qd, J = 4.3, 1.1 Hz, 2H).Compound 111 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(4-hydroxy-4-methylpent-2- ynamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

484.2 1H NMR (400 MHz, DMSO-d6) δ 10.92 (bs, 1H), 9.84 (bs, 1H), 8.76(bs, 1H), 8.36 (bs, 1H), 8.20-7.85 (m, 3H), 7.54 (bs, 1H), 5.87 (bs,1H), 5.75 (s, 1H), 3.88 (s, 3H), 1.67-1.37 (m, 9H). Compound 112(R)-1-(2-chloropyridin-3-yl)ethyl (1-methyl-4-(5-(1-methyl-1H-pyrazole-4- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

482.1 1H NMR (400 MHz DMSO-d6) δ 10.07 (s, 1H), 9.85 (bs, 1H), 8.93 (bs,1H), 8.36 (s, 2H), 8.22-7.98 (m, 3H), 7.94 (d, J = 8.6 Hz, 1H), 7.55(bs, 1H), 5.88 (bs, 1H), 3.92 (s, 3H), 3.88 (s, 3H), 1.57 (bs, 3H).Compound 113 (R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(1H-pyrazole-4-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

468.2 1H NMR (400 MHz, DMSO-d6) δ 13.33 (s, 1H), 10.06 (s, 1H), 9.87(bs, 1H), 8.94 (bs, 1H), 8.36 (bs, 2H), 8.23-7.96 (m, 2H), 7.94 (d, J =8.6 Hz, 1H), 7.55 (bs, 1H), 5.88 (bs, 1H), 3.88 (s, 3H), 1.57 (bs, 3H).Compound 114 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(4-fluorobicyclo[2.2.2]octane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

527.9 1H NMR (400 MHz, DMSO-d6) δ 9.84 (bs, 1H), 9.48 (s, 1H), 8.80 (bs,1H), 8.35 (bs, 1H), 8.20-7.92 (m, 2H), 7.87 (d, J = 8.7 Hz, 1H), 7.53(bs, 1H), 5.87 (bs, 1H), 3.87 (s, 3H), 2.10-1.97 (m, 6H), 1.89- 1.75 (m,6H), 1.56 (bs, 3H). Compound 115 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(4-hydroxybicyclo[2.2.2]octane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

525.9 1H NMR (400 MHz, DMSO-d6) δ 9.84 (bs, 1H), 9.40 (s, 1H), 8.80 (bs,1H), 8.35 (bs, 1H), 8.15-7.92 (m, 2H), 7.86 (d, J = 8.7 Hz, 1H), 7.53(bs, 1H), 5.87 (bs, 1H), 4.36 (s, 1H), 3.87 (s, 3H), 2.01-1.78 (m, 6H),1.78-1.31 (m, 9H). Compound 116 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(1-(difluoromethyl)cyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

491.9 1H NMR (400 MHz, DMSO-d6) δ 9.85 (bs, 1H), 9.64 (s, 1H), 8.77 (s,1H), 8.36 (bs, 1H), 8.16-7.94 (m, 2H), 7.91 (d, J = 8.6 Hz, 1H), 7.53(bs, 1H), 6.58 (t, J = 56.9 Hz, 1H), 5.87 (bs, 1H), 3.87 (s, 3H),1.75-1.27 (m, 5H), 1.28-0.99 (m, 2H). Compound 117(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(3-hydroxybicyclo[1.1.1]pentane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

484.2 1H NMR (400 MHz, DMSO-d6) δ 9.93-9.63 (m, 2H), 8.85 (bs, 1H), 8.36(bs, 1H), 8.18-7.92 (m, 2H), 7.89 (d, J = 8.7 Hz, 1H), 7.51 (bs, 1H),6.42 (s, 1H), 5.87 (bs, 1H), 3.86 (s, 3H), 2.13 (s, 6H), 1.54 (bs, 3H).Compound 118 (R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(3-hydroxy-3-methylbutanamido)pyridin-2-yl)-1- methyl-1H-1,2,3-triazol-5-yl)carbamate

474.2 1H NMR (400 MHz, DMSO-d6) δ 10.10 (s, 1H), 9.83 (bs, 1H), 8.75(bs, 1H), 8.35 (bs, 1H), 8.17-792 (m, 2H), 7.88 (d, J = 8.6 Hz, 1H),7.53 (bs, 1H), 5.86 (bs, 1H), 4.74 (s, 1H), 3.87 (s, 3H), 2.47 (s, 2H),1.46 (bs, 3H), 1.26 (s, 6H). Compound 119(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(1-(difluoromethyl)-3,3-difluorocyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

542.1 1H NMR (400 MHz, Methanol- d4) δ 8.95 (s, 1H), 8.32 (s, 1H), 8.15(m, 2H), 7.95 (d, 1H), 7.50 (s, 1H), 6.33 (t, J = 55.9 Hz, 1H), 6.08 (d,1H), 4.00 (s, 3H), 3.23 (m, 2H), 3.07 (m, 2H), 1.64 (s, 3H). Compound120 (R)-1-(2-chloropyridin-3-yl)ethyl (1- methyl-4-(5-(3-oxo-1-(trifluoromethyl)cyclobutane-1- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

538.1 1H NMR (400 MHz, Methanol- d4) δ 9.13-8.71 (m, 1H), 8.32 (s, 2H),8.24-7.70 (m, 2H), 7.62- 7.33 (m, 1H), 6.08 (d, 1H), 3.96 (m, 5H),3.68-3.46 (m, 1H), 3.08- 2.61 (m, 2H), 1.87-1.40 (m, 3H). Compound 121(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-((1s,3S)-3-cyano-1-methylcyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

495.1 1H NMR (400 MHz, Methanol- d4) δ 9.05 (s, 1H), 8.34 (s, 1H),8.28-8.00 (m, 2H), 7.94 (d, 1H), 7.51 (s, 1H), 6.09 (d, 1H), 4.01 (s,3H), 3.39 (m, 1H), 2.94-2.78 (m, 2H), 2.49-2.34 (m, 2H), 1.58 (m, 6H).Compound 122 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((1r,3R)-3-cyano-1- methylcyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

495.1 1H NMR (400 MHz, Methanol- d4) δ 8.97 (d, 1H), 8.34 (s, 1H),8.27-7.99 (m, 2H), 7.93 (d, 1H), 7.51 (s, 1H), 6.08 (d, 1H), 4.01 (s,3H), 3.28-3.16 (m, 1H), 3.13- 2.96 (m, 2H), 2.49-2.21 (m, 2H), 1.67 (s,6H). Compound 123 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(3-cyano-3-fluorocyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

499.0 1H NMR (400 MHz, Methanol- d4) δ 8.91 (s, 1H), 8.32 (s, 1H),8.23-7.75 (m, 3H), 7.49 (s, 1H), 6.08 (d, 1H), 4.90-4.65 (m, 2H), 4.00(s, 3H), 2.83-2.65 (m, 1H), 1.93-1.80 (m, 2H), 1.55 (d, 3H). Compound124 (R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-((R)-2-hydroxypropanamido)pyridin-2-yl)-1- methyl-1H-1,2,3-triazol-5-yl)carbamate

446.0 1H NMR (400 MHz, Methanol- d4) δ 9.26-8.87 (m, 1H), 8.47- 8.20 (m,2H), 8.20-7.77 (m, 2H), 7.49 (s, 1H), 6.09 (m, 1H), 4.34 (m, 1H), 4.00(s, 3H), 1.86-1.53 (m, 3H), 1.49 (d, 3H). Compound 125(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-((S)-2-hydroxypropanamido)pyridin-2-yl)-1- methyl-1H-1,2,3-triazol-5-yl)carbamate

446.0 1H NMR (400 MHz, Methanol- d4) δ 9.26-8.86 (m, 1H), 8.44- 8.19 (m,2H), 8.19-7.77 (m, 2H), 7.49 (s, 1H), 6.09 (q, 1H), 4.34 (q, 1H), 4.00(s, 3H), 1.63 (s, 3H), 1.48 (d, 3H). Compound 126(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(2-hydroxyacetamido)pyridin-2-yl)- 1-methyl-1H-1,2,3-triazol-5-yl)carbamate

432.0 1H NMR (400 MHz, Methanol- d4) δ 9.01 (s, 1H), 8.51-8.29 (m, 1H),8.23 (dd, 1H), 8.18-7.80 (m, 2H), 7.48 (s, 1H), 6.09 (m, 1H), 4.20 (s,2H), 4.00 (s, 3H), 1.62 (s, 3H). Compound 127(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-((1r,3R)-3-cyanocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

481.1 1H NMR (400 MHz, Methanol- d4) δ 8.96 (d, 1H), 8.33 (s, 1H), 8.12(m, 2H), 7.91 (d, 1H), 7.43 (d, 1H), 6.08 (d, 1H), 3.99 (s, 3H), 3.45(m, 2H), 2.85-2.48 (m, 4H), 1.62 (s, 3H). Compound 128(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-((1s,3S)-3-cyanocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

481.1 1H NMR (400 MHz, Methanol- d4) δ 8.91 (s, 1H), 8.32 (s, 1H),7.91-8.12 (m, 3H), 6.08 (d, 1H), 3.99 (s, 3H), 3.32-3.54 (m, 2H), 2.80(m, 2H), 2.64 (m, 2H), 1.62 (s, 3H). Compound 129(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(2-cyano-2-methylpropanamido)pyridin-2-yl)-1- methyl-1H-1,2,3-triazol-5-yl)carbamate

469.1 1H NMR (400 MHz, Methanol- d4) δ 8.98 (s, 1H), 8.33 (s, 1H), 8.22(m, 1H), 7.97 (m, 2H), 7.48 (s, 1H), 6.09 (m, 1H), 4.01 (s, 3H), 1.75(s, 6H), 1.61 (s, 3H). Compound 130 (R)-1-(2-chloropyridin-3-yl)ethyl(4- (5-(2-cyanocyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

467.1 1H NMR (400 MHz, Methanol- d4) δ 8.99 (s, 1H), 8.44-8.26(m, 1H),8.23-7.85 (m, 3H), 7.47 (s, 1H), 6.08 (m, 1H), 4.00 (s, 3H), 2.49 (m,1H), 2.14 (m, 1H), 1.79- 1.44 (m, 5H). Compound 131(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(1,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

492.1 1H NMR (400 MHz, Methanol- d4) δ 8.96 (d, 1H), 8.45-8.20 (m, 2H),8.20-7.85 (m, 2H), 7.51 (s, 1H), 6.09 (d, 1H), 5.18-4.96 (m, 1H), 4.00(s, 3H), 3.24-3.05 (m, 2H), 2.93-2.59 (m, 2H), 1.61 (d, 3H). Compound132 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(1-cyano-3-fluorocyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

499.1 1H NMR (400 MHz, Methanol- d4) δ 9.11-8.82 (m, 1H), 8.34 (s, 1H),8.23-8.09 (m, 2H), 7.99 (m, 1H), 7.70-7.31 (m, 1H), 6.09 (d, 1H), 5.34(m, 1H), 4.00 (s, 3H), 3.20-2.82 (m, 4H), 1.64 (s, 3H). Compound 133(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-((1r,3R)-1-fluoro-3-hydroxycyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

490.0 1H NMR (400 MHz, Methanol- d4) δ 9.07 (s, 1H), 8.50-8.23 (m, 2H),8.22-7.83 (m, 2H), 7.51 (s, 1H), 6.09 (d, 1H), 4.62 (m, 1H), 4.00 (s,3H), 2.90-2.56 (m, 4H), 1.65 (s, 3H). Compound 134(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-((1s,3S)-1-fluoro-3-hydroxycyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

490.0 1H NMR (400 MHz, Methanol- d4) δ 9.03 (s, 1H), 8.46-8.20 (m, 2H),8.20-7.85 (m, 2H), 7.51 (s, 1H), 6.09 (d, 1H), 4.23 (m, 1H), 4.00 (s,3H), 3.04 (m, 2H), 2.59- 2.34 (m, 2H), 1.64 (s, 3H). Compound 135(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(1-cyano-3-hydroxycyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

497.1 1H NMR (400 MHz, Methanol- d4) δ 8.98 (s, 1H), 8.33 (s, 1H), 8.22(m, 1H), 8.15-7.86 (m, 2H), 7.48 (s, 1H), 6.09 (m, 1H), 4.63- 4.25 (m,1H), 4.01 (s, 3H), 3.18 (m, 1H), 3.06-2.91 (m, 1H), 2.80- 2.56 (m, 2H),1.63 (s, 3H). Compound 136 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(3-hydroxy-3- (trifluoromethyl)cyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

540.1 1H NMR (400 MHz, Methanol- d4) δ 9.03 (s, 1H), 8.33 (s, 1H), 8.19(m, 1H), 8.13-7.85 (m, 2H), 7.49 (s, 1H), 6.09 (m, 1H), 4.01 (s, 3H),3.09 (m, 1H), 2.84-2.68 (m, 2H), 2.65-2.47 (m, 2H), 1.63 (s, 3H).Compound 137 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((1R,2S)-2-cyanocyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

467.1 1H NMR (400 MHz, Methanol- d4) δ 9.24-8.84 (m, 1H), 8.33 (d, 1H),8.25-7.99 (m, 2H), 7.94 (d, 1H), 7.50 (s, 1H), 6.20-5.97 (m, 1H),4.09-3.87 (m, 3H), 2.40 (m, 1H), 2.18 (m, 1H), 1.80-1.43 (m, 5H).Compound 138 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((1s,3S)-3-cyano-3- methoxycyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

511.1 1H NMR (400 MHz, Methanol- d4) δ 9.00 (s, 1H), 8.33 (s, 1H), 8.17(m, 2H), 7.92 (d, 1H), 7.48 (s, 1H), 6.08 (m, 1H), 4.00 (s, 3H), 3.41(s, 3H), 3.29-3.15 (m, 1H), 2.93-2.79 (m, 2H), 2.66 (m, 2H), 1.63 (s,3H). Compound 139 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((1r,3R)-3-cyano-3- methoxycyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

511.1 1H NMR (400 MHz, Methanol- d4) δ 9.02 (s, 1H), 8.34 (s, 1H), 8.17(m, 2H), 7.92 (m, 1H), 7.49 (s, 1H), 6.08 (m, 1H), 4.01 (s, 3H),3.52-3.38 (m, 4H), 3.00- 2.84 (m, 2H), 2.70 (m, 2H), 1.63 (s, 3H).Compound 140 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((1s,3S)-3-cyano-3- hydroxycyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

497.1 1H NMR (400 MHz, Methanol- d4) δ 8.97 (d, 1H), 8.47-8.28 (m, 1H),8.19 (m, 2H), 8.10 (d, 1H), 7.92 (d, 1H), 7.48 (s, 1H), 6.08 (m, 1H),4.00 (s, 3H), 3.19 (m, 1H), 2.94-2.80 (m, 2H), 2.65 (m, 2H), 1.63 (s,3H). Compound 141 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(1-cyano-3-oxocyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

495.0 1H NMR (400 MHz, Methanol- d4) δ 8.92 (s, 1H), 8.32 (s, 1H),8.22-8.08 (m, 2H), 7.96 (d, 1H), 7.48 (s, 1H), 6.09 (m, 1H), 4.00 (s,3H), 3.15-2.74 (m, 4H), 1.62 (s, 3H). Compound 142(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(2-cyanocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

481.1 1H NMR (400 MHz, Methanol- d4) δ 9.17-8.85 (m, 1H), 8.45- 8.28 (m,1H), 8.20 (m, 1H), 8.13- 7.84 (m, 2H), 7.48 (s, 1H), 6.08 (m, 1H), 4.00(s, 3H), 3.65 (m, 2H), 2.50-2.23 (m, 4H), 1.59 (d, 3H). Compound 143(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(2-cyanopropanamido)pyridin-2-yl)- 1-methyl-1H-1,2,3-triazol-5-yl)carbamate

455.0 1H NMR (400 MHz, Methanol- d4) δ 8.91 (d, 1H), 8.33 (s, 1H), 8.15(m, 1H), 7.95 (d, 2H), 7.48 (s, 1H), 6.09 (m, 1H), 4.00 (s, 3H), 3.92(m, 1H), 1.66 (m, 6H). Compound 144 (R)-1-(2-chloropyridin-3-yl)ethyl(4- (5-(3,3-difluoro-1-methylcyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

506.1 1H NMR (400 MHz, Methanol- d4) δ 9.07 (s, 1H), 8.46-8.20 (m, 2H),7.95 (d, 2H), 7.48 (s, 1H), 6.09 (m, 1H), 4.01 (s, 3H), 3.25- 3.05 (m,2H), 2.68-2.46 (m, 2H), 1.64 (s, 6H). Compound 145(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(1,3-dicyano-2,2-dimethylcyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

520.1 1H NMR (400 MHz, Methanol- d4) δ 8.91 (s, 1H), 8.32 (s, 1H), 8.16(m, 2H), 7.95 (m, 1H), 7.46 (s, 1H), 6.08 (m, 1H), 4.00 (s, 3H), 3.04(d, 1H), 1.66 (m, 6H), 1.32 (d, 3H). Compound 146(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(1-cyano-2,2-dimethylcyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

495.1 1H NMR (400 MHz, Methanol- d4) δ 8.98 (s, 1H), 8.33 (s, 1H), 8.22(m, 1H), 7.96 (m, 2H), 7.48 (s, 1H), 6.09 (m, 1H), 4.00 (s, 3H), 1.93(d, 1H), 1.63 (s, 3H), 1.53 (s, 3H), 1.47 (d, 1H), 1.24 (d, 3H).Compound 147 (R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(1-cyano-2-(trifluoromethyl)cyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

535.1 1H NMR (400 MHz, Methanol- d4) δ 8.93 (s, 1H), 8.42-8.27 (m, 1H),8.20 (m, 2H), 8.15-7.86 (m, 1H), 7.47 (s, 1H), 6.09 (m, 1H), 4.00 (s,3H), 3.12-2.95 (m, 1H), 2.25-2.07 (m, 2H), 1.62 (s, 3H). Compound 148(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(1-cyano-2-methylcyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

481.1 1H NMR (400 MHz, Methanol- d4) δ 8.95 (s, 1H), 8.33 (d, 1H), 8.21(dd, 1H), 7.94 (d, 2H), 7.48 (s, 1H), 6.09 (m, 1H), 4.00 (s, 3H),2.16-2.02 (m, 1H), 1.98 (dd, J = 8.9, 4.6 Hz, 1H), 1.63 (s, 3H), 1.44(m, 4H). Compound 149 (R)-1-(2-chloropyridin-3-yl)ethyl (1-methyl-4-(5-(spiro[2.2]pentane-1- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

468.1 1H NMR (400 MHz, Methanol- d4) δ 9.10 (s, 1H), 8.34 (s, 1H),8.30-8.00 (m, 2H), 7.93 (d, J = 8.8 Hz, 1H), 7.51 (s, 1H), 6.09 (q, J =6.6 Hz, 1H), 4.01 (s, 3H), 2.20 (dd, J = 7.4, 4.2 Hz, 1H), 1.83- 1.40(m, 5H), 1.10-0.86 (m, 4H). Compound 150(R)-1-(2-chloropyridin-3-yl)ethyl (1-methyl-4-(5-((S)-5-oxopyrrolidine-3- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

485.1 1H NMR (400 MHz, Methanol- d4) δ 9.05 (s, 1H), 8.43-8.26 (m, 1H),8.25-8.01 (m, 2H), 7.94 (d, J = 8.7 Hz, 1H), 7.47 (d, J = 30.4 Hz, 1H),6.08 (d, J = 7.1 Hz, 1H), 4.01 (s, 3H), 3.79-3.61 (m, 2H), 3.55 (tt, J =8.9, 6.5 Hz, 1H), 2.78- 2.60 (m, 2H), 1.84-1.39 (m, 3H). Compound 151(R)-1-(2-chloropyridin-3-yl)ethyl (1-methyl-4-(5-((S)-5-oxopyrrolidine-2- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

485.1 1H NMR (400 MHz, Methanol- d4) δ 9.01 (s, 1H), 8.31 (d, J = 20.5Hz, 1H), 8.26-8.01 (m, 2H), 7.94 (d, J = 8.7 Hz, 1H), 7.64- 7.38 (m,1H), 6.08 (d, J = 6.5 Hz, 1H), 4.41 (dd, J = 8.7, 4.6 Hz, 1H), 4.01 (s,3H), 2.67-2.35 (m, 3H), 2.27 (d, J = 10.5 Hz, 1H), 1.55 (d, J = 73.8 Hz,3H). Compound 152 (R)-1-(2-chloropyridin-3-yl)ethyl (1-methyl-4-(5-((R)-5-oxopyrrolidine-2- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

485.1 1H NMR (400 MHz, Methanol- d4) δ 8.98 (s, 1H), 8.40-8.25 (m, 1H),8.23-8.01 (m, 2H), 7.93 (d, J = 8.8 Hz, 1H), 7.62-7.40 (m, 1H), 6.08 (d,J = 7.5 Hz, 1H), 4.41 (dd, J = 8.7, 4.6 Hz, 1H), 4.00 (s, 3H), 2.67-2.45(m, 2H), 2.39 (ddd, J = 16.9, 9.7, 5.5 Hz, 1H), 2.31-2.19 (m, 1H),1.82-1.43 (m, 3H). Compound 153 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(1,3-dioxolane-2- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

474.1 1H NMR (400 MHz, Methanol- d4) δ 9.04 (s, 1H), 8.43-8.18 (m, 2H),8.07 (s, 1H), 7.95 (d, J = 8.7 Hz, 1H), 7.48 (s, 1H), 6.09 (q, J = 6.6Hz, 1H), 4.25-4.12 (m, 2H), 4.12-4.03 (m, 2H), 4.00 (s, 3H), 1.63 (s,3H). Compound 154 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((1r,3R)-3-hydroxycyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

472.1 1H NMR (400 MHz, Methanol- d4) δ 9.02 (s, 1H), 8.33 (s, 1H), 8.18(dd, J = 8.7, 2.5 Hz, 2H), 7.92 (d, J = 8.7 Hz, 1H), 7.48 (s, 1H), 6.09(q, J = 6.6 Hz, 1H), 4.58- 4.46 (m, 1H), 4.00 (s, 3H), 3.21 (ttd, J =9.9, 3.8, 1.1 Hz, 1H), 2.70- 2.52 (m, 2H), 2.28 (dtd, J = 12.9, 6.7, 3.0Hz, 2H), 1.63 (s, 3H). Compound 155 (R)-1-(2-chloropyridin-3-yl)ethyl(4- (5-((1s,3S)-3-hydroxycyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

472.1 1H NMR (400 MHz, Methanol- d4) δ 9.02 (s, 1H), 8.44-8.28 (m, 1H),8.25-8.06 (m, 2H), 7.99- 7.87 (m, 1H), 7.48 (s, 1H), 6.09 (q, J = 6.6Hz, 1H), 4.19 (tt, J = 8.3, 6.9 Hz, 1H), 4.00 (s, 3H), 2.77 (tt, J =9.7, 7.4 Hz, 1H), 2.57 (dddd, J = 9.4, 7.2, 5.5, 2.8 Hz, 2H), 2.24 (dtt,J = 11.5, 8.2, 1.4 Hz, 2H), 1.63 (s, 3H). Compound 156(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((1r,3R)-3-methoxycyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

486.1 1H NMR (400 MHz, Methanol- d4) δ 9.04 (s, 1H), 8.34 (s, 1H), 8.18(dd, J = 8.7, 2.4 Hz, 2H), 7.92 (d, J = 8.8 Hz, 1H), 7.51 (s, 1H), 6.09(d, J = 7.4 Hz, 1H), 4.26- 4.10 (m, 1H), 4.01 (s, 3H), 3.29 (s, 3H),3.24 (dddd, J = 9.7, 8.5, 4.3, 1.0 Hz, 1H), 2.65-2.53 (m, 2H), 2.30(dtd, J = 13.0, 6.1, 4.2 Hz, 2H), 1.65 (s, 3H). Compound 157(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((1s,3S)-3-methoxycyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

486.1 1H NMR (400 MHz, Methanol- d4) δ 9.01 (s, 1H), 8.33 (s, 1H), 8.16(dd, J = 8.7, 2.5 Hz, 2H), 7.92 (d, J = 8.7 Hz, 1H), 7.51 (s, 1H), 6.09(d, J = 6.8 Hz, 1H), 4.00 (s, 3H), 3.91 (tt, J = 8.1, 6.7 Hz, 1H), 3.28(s, 3H), 2.85 (tt, J = 9.7, 7.7 Hz, 1H), 2.56 (dddd, J = 12.3, 7.5, 4.0,1.3 Hz, 2H), 2.23 (dddq, J = 11.1, 9.4, 7.9, 1.6 Hz, 2H), 1.65 (s, 3H).Compound 158 (R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-((1R,5R)-3-oxabicyclo[3.1.0]hexane-6- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

484.1 1H NMR (400 MHz, Methanol- d4) δ 8.99 (s, 1H), 8.34 (s, 1H), 8.15(dd, J = 8.7, 2.5 Hz, 2H), 7.92 (d, J = 8.7 Hz, 1H), 7.50 (s, 1H), 6.09(d, J = 7.4 Hz, 1H), 4.03- 3.93 (m, 4H), 3.82 (dd, J = 8.6, 1.8 Hz, 2H),2.31-2.23 (m, 2H), 1.76 (t, J = 3.2 Hz, 1H), 1.65 (s, 3H). Compound 159(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(2-oxabicyclo[3.1.0]hexane-6-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

484.1 1H NMR (400 MHz, Methanol- d4) δ 8.94 (s, 1H), 8.34 (s, 1H), 8.11(dd, J = 8.7, 2.5 Hz, 2H), 7.91 (d, J = 8.7 Hz, 1H), 7.50 (s, 1H), 6.09(d, J = 6.9 Hz, 1H), 4.24 (dd, J = 5.0, 2.7 Hz, 1H), 4.12 (td, J = 9.5,3.0 Hz, 1H), 4.00 (s, 3H), 3.58 (td, J = 9.5, 7.7 Hz, 1H), 2.35- 2.20(m, 2H), 2.20-2.06 (m, 2H), 1.64 (s, 3H). Compound 160(R)-1-(2-chloropyridin-3-yl)ethyl (1-methyl-4-(5-(1-(3-methylisoxazol-5- yl)cyclopropane-1-carboxamido)pyridin-2-yl)-1H-1,2,3- triazol-5-yl)carbamate

523.1 1H NMR (400 MHz, Methanol- d4) δ 8.90 (s, 1H), 8.33 (s, 1H),8.22-8.00 (m, 2H), 7.92 (d, J = 8.7 Hz, 1H), 7.50 (s, 1H), 6.37 (s, 1H),6.08 (d, J = 7.0 Hz, 1H), 4.00 (s, 3H), 2.32 (s, 3H), 1.76 (q, J = 4.3Hz, 2H), 1.58 (d, J = 48.4 Hz, 3H), 1.46 (q, J = 4.3 Hz, 2H). Compound161 (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-((1S,2R)-2-fluorocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

462.1 1H NMR (400 MHz, Methanol- d4) δ 8.77 (s, 1H), 8.24-7.50 (m, 4H),5.95 (d, J = 7.6 Hz, 1H), 3.99 (s, 3H), 2.29 (dddd, J = 17.3, 10.4, 6.6,1.6 Hz, 1H), 1.90-1.24 (m, 5H). Compound 162(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(3-cyanobicyclo[1.1.1]pentane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

495.2 1H NMR (400 MHz, Methanol- d4) δ 8.83 (s, 1H), 8.22-7.58 (m, 4H),5.94 (d, J = 7.0 Hz, 1H), 3.99 (s, 3H), 2.64 (s, 6H), 1.61 (s, 3H).Compound 163 (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(3-fluorobicyclo[1.1.1]pentane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

488.2 1H NMR (400 MHz, Methanol- d4) δ 8.84 (s, 1H), 8.23-7.46 (m, 4H),5.94 (d, J = 6.2 Hz, 1H), 3.99 (s, 3H), 2.47 (d, J = 2.4 Hz, 6H), 1.62(s, 3H). Compound 164 (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-((S)-2,2-difluorocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

480.0 1H NMR (400 MHz, Methanol- d4) δ 8.79 (s, 1H), 8.26-7.50 (m, 4H),5.95 (d, J = 7.2 Hz, 1H), 4.00 (s, 3H), 2.75 (ddd, J = 13.1, 10.8, 7.7Hz, 1H), 2.23-2.07 (m, 1H), 1.98-1.79 (m, 1H), 1.62 (s, 3H). Compound165 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-(1-(difluoromethyl)cyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

494.1 ¹H NMR (400 MHz, DMSO-d₆) δ 9.81 (bs, 1H), 9.63 (s, 1H), 8.70 (s,1H), 8.19 (bs, 1H), 8.08-7.94 (m, 2H), 7.91 (d, J = 8.6 Hz, 1H), 6.58(t, J = 56.9 Hz, 1H), 5.79 (bs, 1H), 3.88 (s, 3H), 1.57 (bs, 3H),1.42-1.30 (m, 2H), 1.25-1.08 (m, 2H). Compound 166(R)-1-(2-chloro-5-fluoropyridin-3- yl)ethyl (4-(5-(1-(difluoromethyl)cyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

510.2 1H NMR (400 MHz, DMSO-d6) δ 9.86 (bs, 1H), 9.63 (s, 1H), 8.73 (bs,1H), 8.42 (bs, 1H), 8.10- 7.82 (m, 3H), 6.58 (t, J = 56.9 Hz, 1H), 5.83(bs, 1H), 3.89 (s, 3H), 1.57 (bs, 3H), 1.43-1.35 (m, 2H), 1.27-1.03 (m,2H). Compound 167 (R)-1-(2-chloro-5-fluoropyridin-3- yl)ethyl (4-(5-(3-cyanobicyclo[1.1.1]pentane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

511.2 ¹H NMR (400 MHz, DMSO-d₆) δ 10.01 (s, 1H), 9.86 (bs, 1H), 8.78 (s,1H), 8.42 (bs, 1H), 8.12-7.80 (m, 3H), 5.83 (bs, 1H), 3.89 (s, 3H), 2.58(s, 6H), 1.56 (bs, 3H). Compound 168 (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl (4-(5-(1-cyanocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

485.2 1H NMR (400 MHz, DMSO-d6) δ 10.28 (s, 1H), 9.89 (bs, 1H), 8.73 (s,1H), 8.43 (bs, 1H), 8.07-7.83 (m, 3H), 5.83 (bs, 1H), 3.89 (s, 3H),1.76-1.67 (m, 4H), 1.57 (bs, 3H). Compound 169(R)-1-(2-fluoropyridin-3-yl)ethyl (4-(5-((1S,2R)-2-fluorocyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

444.1 1H NMR (400 MHz, Methanol- d4) δ 8.79 (s, 1H), 8.43-7.72 (m, 4H),7.35 (s, 1H), 5.99 (q, J = 6.3 Hz, 1H), 3.98 (s, 3H), 2.29 (dddd, J =17.3, 10.5, 6.6, 1.6 Hz, 1H), 1.80-1.46 (m, 4H), 1.40 (dq, J = 13.0, 6.5Hz, 1H). Compound 170 (R)-1-(2-fluoropyridin-3-yl)ethyl (1-methyl-4-(5-(3- (trifluoromethyl)bicyclo[1.1.1]pentane-1-carboxamido)pyridin-2-yl)-1H-1,2,3- triazol-5-yl)carbamate

520.1 1H NMR (400 MHz, Methanol- d4) δ 8.87 (s, 1H), 8.25-7.96 (m, 3H),7.92 (dd, J = 8.6, 0.8 Hz, 1H), 7.36 (s, 1H), 6.10-5.66 (m, 1H), 3.98(s, 3H), 2.39 (s, 6H), 1.62 (s, 3H). Compound 171(R)-1-(2-fluoropyridin-3-yl)ethyl (4- (5-(3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

476.1 ¹H NMR (400 MHz, Methanol-d₄) δ 8.82 (s, 1H), 8.28-8.00 (m, 3H),7.90 (d, J = 8.4 Hz, 1H), 7.54- 7.10 (m, 1H), 6.14-5.79 (m, 1H), 3.98(s, 3H), 3.17-3.13 (m, 1H), 3.03-2.72 (m, 4H), 1.62 (s, 3H). Compound172 (R)-1-(2-fluoropyridin-3-yl)ethyl (4- (5-(1-cyanocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

451.1 1H NMR (400 MHz, Methanol- d4) δ 8.81 (s, 1H), 8.15 (s, 1H), 8.07(dd, J = 8.6, 2.6 Hz, 1H), 7.93 (dd, J = 8.6, 0.8 Hz, 1H), 7.36 (s, 1H),5.99 (d, J = 7.1 Hz, 1H), 3.99 (s, 3H), 1.88-1.42 (m, 8H). Compound 173(R)-1-(2-fluoropyridin-3-yl)ethyl (4-(5-(3-fluorobicyclo[1.1.1]pentane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

470.1 ¹H NMR (400 MHz, Methanol-d₄) δ 8.86(s, 1H), 8.24-8.02 (m, 3H),7.91 (dd, J = 8.7, 0.8 Hz, 1H), 7.51-7.21 (m, 1H), 6.19- 5.83 (m, 1H),3.98 (s, 3H), 2.47 (d, J = 2.4 Hz, 6H), 1.80-1.44 (m, 3H). Compound 174(R)-1-(2-fluoropyridin-3-yl)ethyl (4-(5-(3-cyanobicyclo[1.1.1]pentane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

477.1 ¹H NMR (400 MHz, Methanol-d₄) δ 8.85 (s, 1H), 8.28-7.96 (m, 3H),7.91 (dd, J = 8.7, 0.8 Hz, 1H), 7.35 (s, 1H), 6.14-5.82 (m, 1H), 3.98(s, 3H), 2.64 (s, 6H), 1.62 (s, 3H). Compound 175(R)-1-(5-fluoro-2-methylpyridin-3- yl)ethyl (4-(5-(3,3-difluorocyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

490.1 ¹H NMR (400 MHz, Methanol-d₄) δ 8.78 (s, 1H), 8.25 (s, 1H), 8.10(dd, J = 8.6, 2.6 Hz, 1H), 7.89 (dd, J = 8.7, 0.8 Hz, 1H), 7.84-7.40 (m,1H), 6.14-5.72 (m, 1H), 3.98 (s, 3H), 3.22-3.08 (m, 1H), 3.07- 2.71 (m,4H), 2.56 (s, 3H), 1.80- 1.39 (m, 3H). Compound 176(R)-1-(5-fluoro-2-methylpyridin-3- yl)ethyl (4-(5-((1S,2R)-2-fluorocyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

458.2 1H NMR (400 MHz, Methanol- d4) δ 8.75 (s, 1H), 8.36-7.24 (m, 4H),5.98 (d, J = 6.7 Hz, 1H), 3.97 (s, 3H), 2.56 (s, 3H), 2.29 (dddd, J =17.3, 10.5, 6.6, 1.6 Hz, 1H), 1.81-1.34 (m, 5H). Compound 177(R)-1-(5-fluoro-2-methylpyridin-3- yl)ethyl(4-(5-(1-cyanocyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

465.1 1H NMR (400 MHz, Methanol- d4) δ 8.77 (s, 1H), 8.27 (s, 1H), 8.07(dd, J = 8.6, 2.6 Hz, 1H), 7.92 (dd, J = 8.6, 0.8 Hz, 1H), 7.71 (s, 1H),6.18-5.80 (m, 1H), 3.98 (s, 3H), 2.56 (s, 3H), 1.81- 1.67 (m, 4H), 1.59(s, 3H). Compound 178 (R)-1-(5-fluoro-2-methylpyridin-3- yl)ethyl(4-(5-(3- cyanobicyclo[1.1.1]pentane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

491.1 ¹H NMR (400 MHz, Methanol-d₄) δ 8.81 (s, 1H), 8.26 (s, 1H), 8.09(dd, J = 8.7, 2.6 Hz, 1H), 7.90 (dd, J = 8.6, 0.8 Hz, 1H), 7.86-7.51 (m,1H), 6.10-5.87 (m, 1H), 3.98 (s, 3H), 2.64 (s, 6H), 2.56 (s, 3H), 1.59(s, 3H). Compound 179 (R)-1-(5-fluoro-2-methylpyridin-3- yl)ethyl(4-(5-(3- fluorobicyclo[1.1.1]pentane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

484.1 ¹H NMR (400 MHz, Methanol-d₄) δ 8.82 (s, 1H), 8.26 (s, 1H), 8.10(dd, J = 8.7, 2.6 Hz, 1H), 7.90 (dd, J = 8.6, 0.8 Hz, 1H), 7.86-7.53 (m,1H), 6.11-5.81 (m, 1H), 3.98 (s, 3H), 2.56 (s, 3H), 2.47 (d, J = 2.4 Hz,6H), 1.59 (s, 3H). Compound 180 (R)-1-(5-fluoro-2-methylpyridin-3-yl)ethyl (4-(5-((S)-2,2- difluorocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

476.1 1H NMR (400 MHz, Methanol- d4) δ 8.77 (s, 1H), 8.26 (s, 1H), 8.10(dd, J = 8.7, 2.6 Hz, 1H), 7.91 (dd, J = 8.6, 0.8 Hz, 1H), 7.86-7.49 (m,1H), 6.09-5.82 (m, 1H), 3.98 (s, 3H), 2.75 (ddd, J = 13.2, 10.8, 7.8 Hz,1H), 2.56 (s, 3H), 2.23-2.07 (m, 1H), 1.95- 1.80 (m, 1H), 1.59 (s, 3H).Compound 181 1-(2-chloro-6-fluoropyridin-3-yl)ethyl(4-(5-(1-cyanocyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

485.0 1H NMR (400 MHz, Methanol- d4) δ 8.93 (s, 1H), 8.19 (dd, J = 8.7,2.5 Hz, 2H), 7.97 (d, J = 8.7 Hz, 1H), 7.17 (s, 1H), 6.08 (d, J = 6.8Hz, 1H), 4.00 (s, 3H), 1.86- 1.75 (m, 2H), 1.75-1.67 (m, 2H), 1.63 (s,3H). Compound 182 1-(2-chloro-6-fluoropyridin-3-yl)ethyl(4-(5-acetamidopyridin-2-yl)-1- methyl-1H-1,2,3-triazol-5- yl)carbamate

434.0 1H NMR (400 MHz, Methanol- d4) δ 9.00 (s, 1H), 8.15 (dd, J = 8.7,2.5 Hz, 2H), 7.94 (d, J = 8.7 Hz, 1H), 7.17 (s, 1H), 6.08 (q, J = 6.6Hz, 1H), 4.00 (s, 3H), 2.22 (s, 3H), 1.63 (s, 3H). Compound 183(R)-1-(2-chloropyridin-3-yl)ethyl (4- (5-(1-cyanocyclopropane-1-carboxamido)-4-fluoropyridin-2-yl)-1- methyl-1H-1,2,3-triazol-5-yl)carbamate

485.1 1H NMR (400 MHz, Methanol- d4) δ 8.83 (d, J = 9.7 Hz, 1H), 8.32(d, J = 4.7 Hz, 1H), 8.04 (s, 1H), 7.84 (d, J = 11.1 Hz, 1H), 7.47 (s,1H), 6.16-5.98 (m, 1H), 3.99 (s, 3H), 1.86-1.69 (m, 4H), 1.61 (s, 3H).Compound 184 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(3-cyanobicyclo[1.1.1]pentane-1- carboxamido)-4-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

511.1 1H NMR (400 MHz, Methanol-d4) δ 8.84 (d, J = 9.7 Hz, 1H), 8.32 (d,J = 4.9 Hz, 1H), 8.06 (s, 1H), 7.82 (d, J = 11.3 Hz, 1H), 7.47 (s, 1H),6.21-5.89 (m, 1H), 3.99 (s, 3H), 2.66 (s, 6H), 1.61 (s, 3H). Compound195 (R)-1-(2-chloropyridin-3-yl)ethyl (1-methyl-4-(5-((R)-5-oxopyrrolidine-3- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

485.1 1H NMR (400 MHz, Methanol-d4) δ 9.02 (s, 1H), 8.34 (s, 1H),8.25-8.01 (m, 2H), 7.93 (d, J = 8.8 Hz, 1H), 7.51 (s, 1H), 6.08 (d, J =6.8 Hz, 1H), 4.01 (s, 3H), 3.78-3.62 (m, 2H), 3.54 (tt, J = 8.9, 6.6 Hz,1H), 2.79- 2.60 (m, 2H), 1.65 (s, 3H). Compound 196(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5(2-(1,3-dioxolan-2-yl)acetamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5- yl)carbamate

488.1 1H NMR (400 MHz, Methanol-d4) δ 9.02 (s, 1H), 8.34 (s, 1H), 8.18(dd, J = 8.8, 2.5 Hz, 1H), 8.10 (s, 1H), 7.93 (d, J = 8.7 Hz, 1H), 7.51(s, 1H), 6.09 (q, J = 6.6 Hz, 1H), 5.32 (t, J = 5.0 Hz, 1H), 4.07-4.02(m, 2H), 4.01 (s, 3H), 3.95- 3.89 (m, 2H), 2.80 (d, J = 5.0 Hz, 2H),1.65 (s, 3H). Compound 197 (R)-1-(2-chloropyridin-3-yl)ethyl (1-methyl-4-(5-((1R,2R)-2- phenylcyclopropane-1-carboxamido)pyridin-2-yl)-1H-1,2,3- triazol-5-yl)carbamate

518.2 1H NMR (400 MHz, Methanol-d4) δ 8.85 (s, 1H), 8.43-7.77 (m, 4H),7.65- 7.05 (m, 6H), 6.08 (d, J = 6.8 Hz, 1H), 3.98 (s, 3H), 2.54 (dddd,J = 8.8, 6.3, 4.1, 2.0 Hz, 1H), 2.10 (ddd, J = 8.2, 5.3, 4.1 Hz, 1H),1.80-1.33 (m, 5H). Compound 198 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(3,3-difluoro-1-(pyridin-3- yl)cyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5- yl)carbamate

569.2 1H NMR (400 MHz, Methanol-d4) δ 9.00 (s, 1H), 8.95-8.49 (m, 2H),8.45- 7.71 (m, 5H), 7.50 (s, 1H), 6.05 (s, 1H), 3.99 (s, 3H), 3.71 (m,2H), 3.44-3.35 (m, 2H), 1.63 (s, 3H). Compound 199(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(2,2-difluorospiro[2.2]pentane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

504.1 1H NMR (400 MHz, Methanol-d4) δ 9.01 (s, 1H), 8.33 (s, 1H), 8.17(ddd, J = 8.8, 4.3, 2.4 Hz, 2H), 7.94 (d, J = 8.7 Hz, 1H), 7.51 (s, 1H),6.09 (d, J = 6.8 Hz, 1H), 4.01 (s, 3H), 2.98- 2.90 (m, 1H), 1.65 (s,3H), 1.51 (d, J = 6.4 Hz, 1H), 1.48-1.39 (m, 1H), 1.33 (dq, J = 23.5,7.6, 6.2 Hz, 2H). Compound 200 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(3,3-difluoro-1- (hydroxymethyl)cyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H- 1,2,3-triazol-5-yl)carbamate

522.2 1H NMR (400 MHz, Methanol-d4) δ 9.08 (s, 1H), 8.49-8.21 (m, 2H),8.01 (m, 2H), 7.50 (s, 1H), 6.16- 5.97 (m, 1H), 3.97 (m, 5H), 3.08 (m,2H), 2.70 (m, 2H), 1.63 (s, 3H). Compound 201(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5- ((1R,2R)-1-cyano-2-(trifluoromethyl)cyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

535.1 1H NMR (400 MHz, Methanol-d4) δ 8.88-8.76 (m, 1H), 8.40-8.26 (m,1H), 8.05 (m, 2H), 7.91 (m, 1H), 7.48 (s, 1H), 6.07 (m, 1H), 3.98 (s,3H), 3.10- 2.91 (m, 1H), 2.27-2.08 (m, 2H), 1.62 (s, 3H). Compound 202(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5- ((1S,2S)-1-cyano-2-(trifluoromethyl)cyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

535.1 1H NMR (400 MHz, Methanol-d4) δ 8.84 (s, 1H), 8.39-8.22 (m, 1H),8.05 (m, 2H), 7.92 (m, 1H), 7.46 (m, 1H), 6.07 (m, 1H), 3.98 (s, 3H),3.12-2.95 (m, 1H), 2.24-2.07 (m, 2H), 1.63 (s, 3H). Compound 203(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((R)-2-cyanopropanamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

455.1 1H NMR (400 MHz, Methanol-d4) δ 9.05-8.72 (m, 1H), 8.44-8.23 (m,1H), 8.19-7.79 (m, 3H), 7.44 (m, 1H), 6.07 (m, 1H), 3.99 (s, 3H), 3.92(m, 1H), m 1.81-1.48 (m, 6H). Compound 204(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((S)-2-cyanopropanamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

455.1 1H NMR (400 MHz, Methanol-d4) δ 8.83 (s, 1H), 8.39-8.22 (m, 1H),8.04 (m, 2H), 7.92 (m, 1H), 7.43 (m, 1H), 6.07 (m, 1H), 3.98 (s, 3H),3.95-3.82 (m, 1H), 1.73-1.48 (m, 6H). Compound 205(R)-1-(2-chloropyridin-3-yl)ethyl (1- methyl-4-(5-(2-(trifluoromethyl)pyrimidine-5- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

547.9 1H NMR (400 MHz, Methanol-d4) δ 9.48 (s, 2H), 9.00 (s, 1H), 8.30(s, 1H), 8.21 (dd, J = 8.7, 2.6 Hz, 1H), 8.15-7.88 (m, 2H), 7.47 (s,1H), 6.07 (d, J = 6.7 Hz, 1H), 3.98 (s, 3H), 1.60 (s, 3H). Compound 206(R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(2-(difluoromethyl)pyrimidine-5- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

530.0 1H NMR (400 MHz, Methanol-d4) δ 9.43 (s, 2H), 9.00 (s, 1H), 8.30(s, 1H), 8.21 (dd, J = 8.6, 2.6 Hz, 1H), 8.15-7.84 (m, 2H), 7.47 (s,1H), 6.84 (t, J = 54.2 Hz, 1H), 6.07 (d, J = 6.8 Hz, 1H), 3.98 (s, 3H),1.60 (s, 3H). Compound 207 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (1-methyl-4-(5-((1RS,2RS)-2- methylcyclopropane-1-carboxamido)pyridin-2-yl)-1H-1,2,3- triazol-5-yl)carbamate

458.1 1H NMR (400 MHz, Methanol-d4) δ 8.78 (s, 1H), 8.27-7.50 (m, 4H),5.95 (d, J = 7.6 Hz, 1H), 3.99 (s, 3H), 1.82-1.31 (m, 5H), 1.26- 1.15(m, 4H), 0.76 (ddd, J = 8.0, 6.3, 3.9 Hz, 1H). Compound 208(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4- (5-((1RS,2RS)-2-(fluoromethyl)cyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

476.1 1H NMR (400 MHz, Methanol-d4) δ 8.79 (s, 1H), 8.23-7.52 (m, 4H),5.95 (d, J = 7.3 Hz, 1H),4.53 (ddd, J = 48.7, 10.0, 5.8 Hz, 1H),4.38-4.09 (m, 1H), 3.99 (s, 3H), 1.92-1.79 (m, 2H), 1.62 (s, 3H), 1.31(dq, J = 8.3, 3.8 Hz, 1H), 1.01 (dt, J = 10.8, 5.5 Hz, 1H). Compound 209(R)-1-(2,5-difluoropyridin-3-yl)ethyl (1- methyl-4-(5-((1RS,2RS)-2-(trifluoromethyl)cyclopropane-1- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

512.1 1H NMR (400 MHz, Methanol-d4) δ 8.79 (s, 1H), 8.34-7.48 (m, 4H),5.95 (d, J = 5.6 Hz, 1H), 3.99 (s, 3H), 2.38-2.13 (m, 2H), 1.85- 1.18(m, 5H). Compound 210 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-((1RS,2RS)-2-methoxycyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl- 1H-1,2,3-triazol-5-yl)carbamate

474.2 1H NMR (400 MHz, Methanol-d4) δ 8.77 (s, 1H), 8.32-7.55 (m, 4H),5.95 (d, J = 7.1 Hz, 1H), 3.99 (s, 3H), 3.61 (ddt, J = 6.1, 3.9, 1.8 Hz,1H), 3.44 (d, J = 1.2 Hz, 3H), 1.96 (ddd, J = 9.5, 5.8, 2.0 Hz, 1H),1.62 (s, 3H), 1.38-1.19 (m, 2H). Compound 211(R)-1-(2,5-difluoropyridin-3-yl)ethyl (1- methyl-4-(5-((1RS,2RS)-2-nitrocyclopropane-1- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

489.1 1H NMR (400 MHz, Methanol-d4) δ 8.78 (s, 1H), 8.34-7.55 (m, 4H),5.94 (d, J = 6.7 Hz, 1H), 4.77-4.63 (m, 1H), 3.99 (s, 3H), 2.96 (ddd, J= 10.0, 7.1, 2.7 Hz, 1H), 2.17-2.02 (m, 1H), 1.84 (tdd, J = 7.1, 5.7,1.1 Hz, 1H), 1.61 (s, 3H). Compound 212(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-(6-chloronicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

515.0 1H NMR (400 MHz, Methanol-d4) δ 9.03-8.85 (m, 2H), 8.35 (dd, J =8.3, 2.5 Hz, 1H), 8.23 (dd, J = 8.6, 2.6 Hz, 1H), 8.02 (s, 1H),7.99-7.72 (m, 2H), 7.64 (dd, J = 8.3, 0.7 Hz, 1H), 5.94 (d, J = 7.0 Hz,1H), 3.99 (s, 3H), 1.60 (s, 3H). Compound 213(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-(2-fluoroisonicotinamido)pyridin-2- yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

499.1 1H NMR (400 MHz, Methanol-d4) δ 8.95 (s, 1H), 8.42 (d, J = 5.2 Hz,1H), 8.24 (dd, J = 8.7, 2.6 Hz, 1H), 8.02 (s, 1H), 7.97 (dd, J = 8.6,0.7 Hz, 1H), 7.94- 7.68 (m, 2H), 7.59 (d, J = 1.8 Hz, 1H), 5.94 (d, J =6.7 Hz, 1H), 3.99 (s, 3H), 1.60 (s, 3H). Compound 214(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-(3-(difluoromethyl)oxetane-3- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

510.2 1H NMR (400 MHz, Methanol-d4) δ 8.83 (s, 1H), 8.28-7.35 (m, 4H),6.43 (t, J = 55.6 Hz, 1H), 5.95 (d, J = 6.8 Hz, 1H), 5.03 (dt, J = 7.0,1.8 Hz, 2H), 4.85 (d, J = 7.0 Hz, 2H), 4.00 (s, 3H), 1.62 (s, 3H).Compound 215 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (1- methyl-4-(5-(3-(methylsulfonyl)bicyclo[1.1.1]pentane-1-carboxamido)pyridin-2-yl)-1H-1,2,3- triazol-5-yl)carbamate

548.1 1H NMR (400 MHz, Methanol-d4) δ 8.85 (s, 1H), 8.22-7.49 (m, 4H),5.95 (d, J = 7.2 Hz, 1H), 4.00 (s, 3H), 2.99 (s, 3H), 2.58 (s, 6H), 1.62(s, 3H). Compound 216 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-((1RS,2RS)-2- (difluoromethyl)cyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl-1H- 1,2,3-triazol-5-yl)carbamate

519.1 1H NMR (400 MHz, Methanol-d4) δ 8.86 (s, 1H), 8.16 (m, 1H),8.12-7.72 (m, H), 6.20-5.96 (m, 2H), 4.01 (s, 3H), 2.61 (m, 1H),2.13-1.96 (m, 2H), 1.65 (s, 3H). Compound 217(R)-1-(2,5-difluoropyridin-3-yl)ethyl (1-methyl-4-(5-((1RS,2RS)-2-(pyridin-4-yl)cyclopropane-1-carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

521.1 1H NMR (400 MHz, Methanol-d4) δ 8.79 (s, 1H), 8.47-8.36 (m, 2H),8.16- 7.77 (m, 4H), 7.31-7.23 (m, 2H), 5.95 (d, J = 7.3 Hz, 1H), 3.99(s, 3H), 2.56 (ddd, J = 9.1, 6.3, 4.0 Hz, 1H), 2.25 (ddd, J = 8.5, 5.5,4.0 Hz, 1H), 1.83-1.35 (m, 5H). Compound 218(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4(5-((1S,2R)-2-chlorocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl-1H- 1,2,3-triazol-5-yl)carbamate

478.2 1H NMR (400 MHz, Methanol-d4) δ 8.79 (s, 1H), 8.24-7.51 (m, 4H),5.95 (d, J = 7.4 Hz, 1H), 3.99 (s, 3H), 2.36 (ddd, J = 8.6, 5.7, 3.7 Hz,1H), 2.18-2.07 (m, 1H), 1.89-1.33 (m, 5H). Compound 219(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4- (5-(5-(difluoromethyl)nicotinamido)pyridin-2- yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

531.1 1H NMR (400 MHz, Methanol-d4) δ 9.34-9.18 (m, 1H), 9.01-8.90 (m,2H), 8.58 (s, 1H), 8.26 (dd, J = 8.6, 2.6 Hz, 1H), 8.02 (s, 1H),8.00-7.75 (m, 2H), 7.05 (t, J = 55.3 Hz, 1H), 5.95 (d, J = 7.3 Hz, 1H),3.99 (s, 3H), 1.60 (s, 3H). Compound 220(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-(6-fluoronicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

499.1 1H NMR (400 MHz, Methanol-d4) δ 8.94 (s, 1H), 8.83 (d, J = 2.5 Hz,1H), 8.50 (ddd, J = 8.6, 7.5, 2.6 Hz, 1H), 8.23 (dd, J = 8.6, 2.6 Hz,1H), 8.02 (s, 1H), 7.98-7.67 (m, 2H), 7.24 (dd, J = 8.6, 2.5 Hz, 1H),5.94 (d, J = 7.0 Hz, 1H), 3.99 (s, 3H), 1.61 (s, 3H). Compound 221(R)-1-(2,5-difluoropyridin-3-yl)ethyl (1- methyl-4-(5-(6-methylnicotinamido)pyridin-2-yl)-1H- 1,2,3-triazol-5-yl)carbamate

495.1 1H NMR (400 MHz, Methanol-d4) δ 9.01 (d, J = 2.4 Hz, 1H), 8.94 (s,1H), 8.29 (dd, J = 8.2, 2.4 Hz, 1H), 8.23 (dd, J = 8.6, 2.6 Hz, 1H),8.02 (s, 1H), 7.99- 7.66 (m, 2H), 7.48 (d, J = 8.2 Hz, 1H), 5.94 (d, J =6.5 Hz, 1H), 3.99 (s, 3H), 2.64 (s, 3H), 1.61 (s, 3H). Compound 222(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4- (5-(6-(difluoromethyl)nicotinamido)pyridin-2- yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

531.1 1H NMR (400 MHz, Methanol-d4) δ 9.19 (s, 1H), 8.96 (s, 1H), 8.52(dd, J = 8.1, 2.2 Hz, 1H), 8.25 (dd, J = 8.6, 2.6 Hz, 1H), 8.02 (s, 1H),7.97 (d, J = 8.7 Hz, 1H), 7.90-7.61 (m, 2H), 6.82 (t, J = 55.0 Hz, 1H),5.94 (d, J = 7.3 Hz, 1H), 3.99 (s, 3H), 1.60 (s, 3H). Compound 223(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-(2-methoxyisonicotinamido)pyridin-2- yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

511.1 1H NMR (400 MHz, Methanol-d4) δ 8.94 (s, 1H), 8.32 (dd, J = 5.3,0.8 Hz, 1H), 8.22 (dd, J = 8.6, 2.6 Hz, 1H), 8.02 (s, 1H), 8.00- 7.71(m, 2H), 7.43 (dd, J = 5.3, 1.5 Hz, 1H), 7.31 (dd, J = 1.5, 0.8 Hz, 1H),5.94 (d, J = 7.0 Hz, 1H), 4.06-3.92 (m, 6H), 1.60 (s, 3H). Compound 224(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4- (5-(2-(difluoromethyl)isonicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5- yl)carbamate

531.1 1H NMR (400 MHz, Methanol-d4) δ 8.97 (s, 1H), 8.86 (d, J = 5.1 Hz,1H), 8.32-8.19 (m, 2H), 8.10- 8.01 (m, 2H), 8.00-7.75 (m, 2H), 6.85 (t,J = 55.1 Hz, 1H), 5.94 (d, J = 6.4 Hz, 1H), 3.99 (s, 3H), 1.61 (s, 3H).Compound 225 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (1- methyl-4-(5-(2-(trifluoromethyl)isonicotinamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

549.1 1H NMR (400 MHz, Methanol-d4) δ 9.10-8.85 (m, 2H), 8.35 (t, J =1.2 Hz, 1H), 8.26 (dd, J = 8.6, 2.6 Hz, 1H), 8.16 (dd, J = 5.0, 1.6 Hz,1H), 8.02 (s, 1H), 8.01-7.66 (m, 2H), 5.94 (d, J = 6.4 Hz, 1H), 3.99 (s,3H), 1.61 (s, 3H). Compound 226 (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4- (5-(3,3-difluoro-1-methylcyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H- 1,2,3-triazol-5-yl)carbamate

508.0 1H NMR (400 MHz, Methanol-d4) δ 9.04 (s, 1H), 8.42-8.18 (m, 1H),8.06 (s, 1H), 7.96 (m, 2H), 5.96 (m, 1H), 4.02 (s, 3H), 3.27- 2.96 (m,2H), 2.70-2.41 (m, 2H), 1.64 (s, 6H). Compound 227(R)-1-(2,5-difluoropyridin-3-yl)ethyl (1-methyl-4-(5-(4-methylisoxazole-5- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

485.1 1H NMR (400 MHz, DMSO-d6) δ 10.98 (bs, 1H), 9.82 (bs, 1H), 8.89(bs, 1H), 8.75 (s, 1H), 8.29-7.25 (m, 4H), 5.80 (bs, 1H), 3.89 (s, 3H),2.32 (s, 3H), 1.40 (bs, 3H). Compound 228(R)-1-(2,5-difluoropyridin-3-yl)ethyl (1- methyl-4-(5-(3-methyl-1,1-dioxidothietane-3-carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

522.1 1H NMR (400 MHz, Methanol-d4) δ 8.81 (s, 1H), 8.23-7.60 (m, 4H),5.95 (d, J = 7.0 Hz, 1H), 4.80-4.68 (m, 2H), 4.14-3.91 (m, 5H), 1.86 (s,3H), 1.62 (s, 3H). Compound 229 (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4- (5-((1RS,5SR,6SR)-3,3-dioxido-3- thiabicyclo[3.1.0]hexane-6-carboxamido)pyridin-2-yl)-1-methyl-1H- 1,2,3-triazol-5-yl)carbamate

534.1 1H NMR (400 MHz, Methanol-d4) δ 8.77 (s, 1H), 8.27-7.62 (m, 4H),5.95 (d, J = 6.4 Hz, 1H), 4.00 (s, 3H), 3.61-3.44 (m, 2H), 2.46- 2.31(m, 2H), 2.29-2.18 (m, 1H), 1.62 (s, 3H). Compound 230(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4- (5-((1RS,5SR,6SR)-3,3-difluorobicyclo[3.1.0]hexane-6- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

520.2 1H NMR (400 MHz, Methanol-d4) δ 8.77 (s, 1H), 8.18-7.59 (m, 4H),6.09- 5.77 (m, 1H), 3.99 (s, 3H), 2.55 (dtd, J = 23.8, 14.4, 3.1 Hz,2H), 2.31 (dd, J = 19.4, 14.9 Hz, 2H), 2.13-1.99 (m, 2H), 1.85 (q, J =3.0 Hz, 1H), 1.61 (s, 3H). Compound 231(R)-1-(2,5-difluoropyridin-3-yl)ethyl (1-methyl-4-(5-(6-methylpyridazine-4- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

496.1 1H NMR (400 MHz, Methanol-d4) δ 9.49 (d, J = 2.1 Hz, 1H), 8.96 (s,1H), 8.25 (dd, J = 8.6, 2.6 Hz, 1H), 8.09 (d, J = 2.1 Hz, 1H), 8.03 (s,1H), 8.02- 7.70 (m, 2H), 5.94 (d, J = 6.7 Hz, 1H), 3.99 (s, 3H), 2.83(s, 3H), 1.61 (s, 3H). Compound 232(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-(2-aminoisonicotinamido)pyridin-2- yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

496.1 1H NMR (400 MHz, Methanol-d4) δ 8.93 (s, 1H), 8.21 (dd, J = 8.6,2.6 Hz, 1H), 8.09-8.05 (m, 1H), 8.03 (s, 1H), 7.99-7.76 (m, 2H),7.10-6.96 (m, 2H), 5.94 (d, J = 7.1 Hz, 1H), 3.99 (s, 2H), 1.61 (s, 3H).Compound 233 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (1-methyl-4-(5-(pyrimidine-5- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

482.1 1H NMR (400 MHz, Methanol-d4) δ 9.39-9.23 (m, 3H), 8.95 (s, 1H),8.25 (dd, J = 8.7, 2.6 Hz, 1H), 8.03 (s, 1H), 8.00-7.91 (m, 2H), 5.95(d, J = 7.1 Hz, 1H), 3.99 (s, 3H), 1.61 (s, 3H). Compound 234(R)-1-(2,5-difluoropyridin-3-yl)ethyl (1-methyl-4-(5-(2-methylpyrimidine-5- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

496.1 1H NMR (400 MHz, Methanol-d4) δ 9.21 (s, 2H), 8.94 (s, 1H), 8.23(dd, J = 8.7, 2.6 Hz, 1H), 8.03 (s, 1H), 8.00-7.91 (m, 2H), 5.94 (d, J =7.5 Hz, 1H), 3.99 (s, 3H), 2.79 (s, 3H), 1.61 (s, 3H). Compound 235(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4- (5-(2-cyanopyrimidine-5-carboxamido)pyridin-2-yl)-1-methyl-1H- 1,2,3-triazol-5-yl)carbamate

507.1 1H NMR (400 MHz, DMSO-d6) δ 11.01 (s, 1H), 9.87 (s, 1H), 9.48 (s,2H), 8.88 (s, 1H), 8.21 (dd, J = 8.6, 2.6 Hz, 2H), 8.07-7.86 (m, 2H),5.81 (s, 1H), 3.90 (s, 3H), 1.55 (s, 3H). Compound 236(R)-1-(2,5-difluoropyridin-3-yl)ethyl (1-methyl-4-(5-(1-methyl-6-oxo-1,6- dihydropyridine-3-carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

511.1 1H NMR (400 MHz, Methanol-d4) δ 8.89 (s, 1H), 8.50 (d, J = 2.6 Hz,1H), 8.17 (dd, J = 8.6, 2.6 Hz, 1H), 8.07 (dd, J = 9.5, 2.7 Hz, 1H),8.02 (s, 1H), 7.97- 7.73 (m, 2H), 6.61 (d, J = 9.5 Hz, 1H), 5.94 (d, J =7.1 Hz, 1H), 3.99 (s, 3H), 3.66 (s, 3H), 1.61 (s, 3H). Compound 237(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-((1RS,2RS)-2-(6-fluoropyridin-3-yl)cyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5- yl)carbamate

539.0 1H NMR (400 MHz, Methanol-d4) δ 8.79 (s, 1H), 8.21-7.66 (m, 6H),7.04 (dd, J = 8.5, 2.6 Hz, 1H), 5.94 (d, J = 6.9 Hz, 1H), 3.99 (s, 3H),2.60 (dt, J = 10.1, 5.4 Hz, 1H), 2.14 (ddd, J = 8.3, 5.2, 4.1 Hz, 1H),1.84-1.34 (m, 5H). Compound 238 (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4- (5-((1RS,2RS)-2-(3-chloropyridin-4-yl)cyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5- yl)carbamate

555.0 1H NMR (400 MHz, Methanol-d4) δ 8.80 (s, 1H), 8.55 (s, 1H), 8.42(d, J = 5.1 Hz, 1H), 8.25-7.51 (m, 4H), 7.20 (d, J = 5.2 Hz, 1H), 5.95(d, J = 6.3 Hz, 1H), 4.00 (s, 3H), 2.84 (dddd, J = 8.6, 6.3, 4.4, 1.5Hz, 1H), 2.24-2.10 (m, 1H), 1.90-1.31 (m, 5H). Compound 239(R)-1-(2,5-difluoropyridin-3-yl)ethyl (1-methyl-4-(5-(4-methyl-1,2,5-oxadiazole-3-carboxamido)pyridin-2-yl)-1H-1,2,3- triazol-5-yl)carbamate

486.0 1H NMR (400 MHz, DMSO-d6) δ 11.33 (bs, 1H), 9.82 (bs, 1H), 8.88(s, 1H), 8.29-8.10 (m, 2H), 8.10- 7.74 (m, 2H), 5.80 (bs, 1H), 3.90 (s,3H), 2.58 (s, 3H), 1.56 (bs, 3H). Compound 240(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4- (5-((1r,3R)-3-cyano-1-methylcyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

497.1 1H NMR (400 MHz, Methanol-d4) δ 9.03 (s, 1H), 8.27 (m, 1H),8.13-7.74 (m, 3H), 5.95 (m, 1H), 4.01 (s, 3H), 3.28-3.13 (m, 1H),3.11-2.98 (m, 2H), 2.35 (m, 2H), 1.66 (s, 6H). Compound 241(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-(2,5-difluoronicotinamido)pyridin-2- yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

517.0 1H NMR (400 MHz, Methanol-d4) δ 8.89 (s, 1H), 8.31 (dd, J = 3.1,1.7 Hz, 1H), 8.25-8.10 (m, 2H), 8.03 (s, 1H), 8.01-7.93 (m, 2H), 5.94(d, J = 6.7 Hz, 1H), 3.99 (s, 3H), 1.60 (s, 3H). Compound 242(R)-1-(2,5-difluoropyridin-3-yl)ethyl (1- methyl-4-(5-(6-(trifluoromethyl)nicotinamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

549.0 1H NMR (400 MHz, Methanol-d4) δ 9.25 (d, J = 2.1 Hz, 1H),9.06-8.84 (m, 1H), 8.56 (dd, J = 8.2, 2.1 Hz, 1H), 8.23 (dd, J = 8.6,2.6 Hz, 1H), 8.02 (s, 1H), 7.99 (d, J = 8.1 Hz, 1H), 7.98-7.72 (m, 2H),5.95 (d, J = 7.3 Hz, 1H), 3.99 (s, 3H), 1.61 (s, 3H). Compound 243(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-(2,3-difluoroisonicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5- yl)carbamate

516.9 1H NMR (400 MHz, Methanol-d4) δ 8.88 (s, 1H), 8.21 (dd, J = 8.6,2.6 Hz, 1H), 8.14 (dd, J = 5.0, 1.4 Hz, 1H), 8.08-7.69 (m, 3H), 7.61(dd, J = 5.0, 4.1 Hz, 1H), 5.94 (d, J = 6.9 Hz, 1H), 3.99 (s, 3H), 1.60(s, 3H). Compound 244 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-(2,6-difluoroisonicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5- yl)carbamate

516.9 1H NMR (400 MHz, Methanol-d4) δ 8.94 (s, 1H), 8.23 (dd, J = 8.7,2.6 Hz, 1H), 8.12-7.67 (m, 3H), 7.52 (s, 2H), 5.94 (d, J = 7.0 Hz, 1H),3.99 (s, 3H), 1.60 (s, 3H). Compound 245(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4- (5-((1R,2R)-1-cyano-2-(difluoromethyl)cyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

519.1 1H NMR (400 MHz, Methanol-d4) δ 8.79 (s, 1H), 8.16-7.99 (m, 2H),7.93 (m, 2H), 6.20-5.93 (m, 2H), 3.99 (s, 3H), 2.66-2.48 (m, 1H),2.10-1.90 (m, 2H), 1.61 (s, 3H). Compound 246(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4- (5-((1S,2S)-1-cyano-2-(difluoromethyl)cyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

519.1 1H NMR (400 MHz, Methanol-d4) δ 8.80 (s, 1H), 8.15-7.99 (m, 2H),7.98- 7.83 (m, 2H), 6.20-5.94 (m, 2H), 3.99 (s, 3H), 2.59 (m, 1H),2.10-1.92 (m, 2H), 1.61 (s, 3H). Compound 247(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4- (5-((1RS,3RS)-2,2-difluoro-3-phenylcyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

556.0 1H NMR (400 MHz, Methanol-d4) δ 8.82 (s, 1H), 8.31-7.66 (m, 4H),7.49- 7.24 (m, 5H), 5.95 (d, J = 7.5 Hz, 1H), 4.00 (s, 3H), 3.65 (ddd, J= 11.7, 7.8, 5.1 Hz, 1H), 3.09 (ddd, J = 11.2, 7.9, 3.0 Hz, 1H), 1.62(s, 3H). Compound 248 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-((1RS,2SR)-3,3-difluoro-[1,1′- bi(cyclopropane)]-2-carboxamido)pyridin-2-yl)-1-methyl-1H- 1,2,3-triazol-5-yl)carbamate

520.0 1H NMR (400 MHz, Methanol-d4) δ 8.76 (s, 1H), 8.26-7.59 (m, 4H),5.94 (d, J = 7.0 Hz, 1H), 3.99 (s, 3H), 2.44 (dd, J = 13.2, 7.4 Hz, 1H),2.26 (dtd, J = 13.6, 7.0, 3.6 Hz, 1H), 1.61 (s, 3H), 1.07-0.82 (m, 1H),0.81- 0.53 (m, 2H), 0.53-0.24 (m, 2H). Compound 249(R)-1-(2,5-difluoropyridin-3-yl)ethyl (1-methyl-4-(5-(2-methylpyrimidine-4- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

496.0 1H NMR (400 MHz, Methanol-d4) δ 9.05 (s, 1H), 8.97 (d, J = 5.1 Hz,1H), 8.35 (dd, J = 8.6, 2.6 Hz, 1H), 8.10-7.70 (m, 4H), 5.95 (d, J = 6.5Hz, 1H), 3.99 (s, 3H), 2.86 (s, 3H), 1.61 (s, 3H). Compound 250(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4- (5-(6-chloropyridazine-3-carboxamido)pyridin-2-yl)-1-methyl-1H- 1,2,3-triazol-5-yl)carbamate

516.0 1H NMR (400 MHz, Methanol-d4) δ 9.06 (s, 1H), 8.41 (d, J = 8.8 Hz,1H), 8.35 (dd, J = 8.7, 2.6 Hz, 1H), 8.04 (t, J = 6.6 Hz, 2H), 8.01-7.95(m, 2H), 5.95 (d, J = 7.0 Hz, 1H), 3.99 (s, 3H), 1.61 (s, 3H). Compound251 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (1- methyl-4-(5-(2-(trifluoromethyl)pyrimidine-5- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

550.0 1H NMR (400 MHz, Methanol-d4) δ 9.47 (s, 2H), 8.95 (s, 1H), 8.25(dd, J = 8.6, 2.6 Hz, 1H), 8.03 (s, 1H), 7.98 (dd, J = 8.7, 0.7 Hz, 1H),7.87 (s, 1H), 5.95 (d, J = 7.1 Hz, 1H), 3.99 (s, 3H), 1.61 (s, 3H).Compound 252 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-(2-(difluoromethyl)pyrimidine-5-carboxamido)pyridin-2-yl)-1-methyl-1H- 1,2,3-triazol-5-yl)carbamate

532.0 1H NMR (400 MHz, Methanol-d4) δ 9.42 (s, 2H), 9.01-8.87 (m, 1H),8.25 (dd, J = 8.7, 2.6 Hz, 1H), 8.03 (s, 1H), 7.98 (dd, J = 8.7, 0.8 Hz,1H), 7.83 (d, J = 45.1 Hz, 1H), 6.84 (t, J = 54.1 Hz, 1H), 5.95 (d, J =6.8 Hz, 1H), 3.99 (s, 3H), 1.61 (s, 3H). Compound 253(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-(4-chloronicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

515.0 1H NMR (400 MHz, Methanol-d4) δ 8.88 (s, 1H), 8.78 (s, 1H), 8.62(d, J = 5.5 Hz, 1H), 8.21 (dd, J = 8.7, 2.6 Hz, 1H), 8.02 (s, 1H),8.00-7.94 (m, 2H), 7.66 (d, J = 5.5 Hz, 1H), 5.94 (d, J = 6.6 Hz, 1H),3.99 (s, 3H), 1.60 (s, 3H). Compound 254(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4- (5-(2-fluoro-6-(trifluoromethyl)nicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5- yl)carbamate

566.9 1H NMR (400 MHz, Methanol-d4) δ 8.89 (s, 1H), 8.54 (t, J = 8.1 Hz,1H), 8.22 (dd, J = 8.7, 2.6 Hz, 1H), 8.03 (s, 1H), 7.98 (dd, J = 8.7,0.8 Hz, 1H), 7.95-7.87 (m, 2H), 5.94 (d, J = 6.7 Hz, 1H), 3.99 (s, 3H),1.61 (s, 3H). Compound 255 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-(4,6-difluoronicotinamido)pyridin-2- yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

517.0 1H NMR (400 MHz, Methanol-d4) δ 8.88 (s, 1H), 8.65 (d, J = 9.7 Hz,1H), 8.21 (dd, J = 8.7, 2.6 Hz, 1H), 8.02 (s, 1H), 8.00- 7.73 (m, 2H),7.16 (dd, J = 9.8, 1.7 Hz, 1H), 5.94 (d, J = 7.1 Hz, 1H), 3.99 (s, 3H),1.61 (s, 3H). Compound 256 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (1-methyl-4-(5-(2-methyloxazole-5- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

485.0 1H NMR (400 MHz, DMSO-d6) δ 10.59 (bs, 1H), 9.82 (bs, 1H), 8.85(bs, 1H), 8.36-8.12 (m, 2H), 8.11- 7.83 (m, 3H), 5.80 (bs, 1H), 3.89 (s,3H), 2.56 (s, 3H), 1.57 (bs, 3H). Compound 257(R)-1-(2,5-difluoropyridin-3-yl)ethyl (1-methyl-4-(5-(5-methyl-1,3,4-oxadiazole-2-carboxamido)pyridin-2-yl)-1H-1,2,3- triazol-5-yl)carbamate

486.0 1H NMR (400 MHz, DMSO-d6) δ 11.47 (bs, 1H), 9.80 (bs, 1H), 8.91(s, 1H), 8.39-8.11 (m, 2H), 8.11- 7.64 (m, 2H), 5.80 (bs, 1H), 3.89 (s,3H), 2.65 (s, 3H), 1.38 (d, J = 118.8 Hz, 3H). Compound 258(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4- (5-(3-cyanoisoxazole-5-carboxamido)pyridin-2-yl)-1-methyl-1H- 1,2,3-triazol-5-yl)carbamate

495.9 1H NMR (400 MHz, DMSO-d6) δ 11.29 (bs, 1H), 9.83 (bs, 1H), 8.87(s, 1H), 8.38-7.56 (m, 5H), 5.80 (bs, 1H), 3.90 (s, 3H), 1.56 (bs, 3H).Compound 259 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (1- methyl-4-(5-(6-(trifluoromethyl)pyridazine-4- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

550.0 1H NMR (400 MHz, Methanol-d4) δ 9.91 (d, J = 2.0 Hz, 1H), 8.97 (s,1H), 8.63 (d, J = 2.1 Hz, 1H), 8.27 (dd, J = 8.7, 2.6 Hz, 1H), 8.03 (s,1H), 8.01- 7.64 (m, 2H), 5.95 (d, J = 7.0 Hz, 1H), 3.99 (s, 3H), 1.61(s, 3H). Compound 260 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (1-methyl-4-(5-(3-methylisoxazole-5- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

485.0 1H NMR (400 MHz, DMSO-d6) δ 10.99 (bs, 1H), 9.82 (bs, 1H), 8.89(s, 1H), 8.38-7.69 (m, 4H), 7.16 (s, 1H), 5.78 (bs, 1H), 3.89 (s, 3H),2.36 (s, 3H), 1.56 (bs, 3H). Compound 261(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4- (5-(3-fluoro-2-(trifluoromethyl)isonicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5- yl)carbamate

567.0 1H NMR (400 MHz, Methanol-d4) δ 8.89 (s, 1H), 8.69 (d, J = 4.8 Hz,1H), 8.21 (dd, J = 8.6, 2.6 Hz, 1H), 8.07-7.76 (m, 4H), 5.94 (d, J = 6.8Hz, 1H), 3.99 (s, 3H), 1.60 (s, 3H). Compound 262(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4- (5-(6-chloro-2-fluoronicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

533.0 1H NMR (400 MHz, Methanol-d4) δ 8.88 (s, 1H), 8.32 (dd, J = 9.1,7.9 Hz, 1H), 8.20 (dd, J = 8.7, 2.6 Hz, 1H), 8.02 (s, 1H), 8.00- 7.75(m, 2H), 7.56 (dd, J = 7.9, 1.1 Hz, 1H), 5.94 (d, J = 7.1 Hz, 1H), 3.99(s, 3H), 1.60 (s, 3H). Compound 263(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4- (5-(4-chloro-5-fluoronicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

533.0 1H NMR (400 MHz, Methanol-d4) δ 8.88 (s, 1H), 8.71 (d, J = 1.1 Hz,1H), 8.65 (s, 1H), 8.21 (dd, J = 8.6, 2.6 Hz, 1H), 8.02 (s, 1H),8.00-7.76 (m, 2H), 5.94 (d, J = 7.1 Hz, 1H), 3.99 (s, 3H), 1.61 (s, 3H).Compound 264 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (1-methyl-4-(5-(2,3,6- trifluoroisonicotinamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

535.0 1H NMR (400 MHz, Methanol-d4) δ 8.87 (s, 1H), 8.20 (dd, J = 8.6,2.6 Hz, 1H), 8.07-7.71 (m, 3H), 7.36 (t, J = 2.9 Hz, 1H), 5.94 (d, J =6.3 Hz, 1H), 3.99 (s, 3H), 1.60 (s, 3H). Compound 265(R)-1-(2,5-difluoropyridin-3-yl)ethyl (1-methyl-4-(5-((1R,2R)-2-(pyridin-2-yl)cyclopropane-1-carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

521.0 1H NMR (400 MHz, Methanol-d4) δ 8.80 (s, 1H), 8.58-8.32 (m, 1H),8.27- 7.60 (m, 5H), 7.40 (dd, J = 7.9, 1.0 Hz, 1H), 7.24 (ddd, J = 7.5,4.9, 1.1 Hz, 1H), 5.95 (s, 1H), 3.99 (s, 3H), 2.68 (ddd, J = 9.5, 6.2,3.9 Hz, 1H), 2.51-2.28 (m, 1H), 1.85-1.51 (m, 5H). Compound 266(R)-1-(2,5-difluoropyridin-3-yl)ethyl (1-methyl-4-(5-((1S,2S)-2-(pyridin-2-yl)cyclopropane-1-carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

521.0 1H NMR (400 MHz, Methanol-d4) δ 8.80 (s, 1H), 8.52-8.38 (m, 1H),8.22- 7.60 (m, 5H), 7.48-7.32 (m, 1H), 7.24 (ddd, J = 7.6, 5.0, 1.2 Hz,1H), 5.95 (s, 1H), 3.99 (s, 3H), 2.68 (ddd, J = 9.3, 6.1, 3.8 Hz, 1H),2.39 (ddd, J = 9.1, 5.5, 3.9 Hz, 1H), 1.82-1.50 (m, 5H). Compound 267(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-((1S,2R)[1,1′-bi(cyclopropane)]-2-carboxamido)pyridin-2-yl)-1-methyl-1H- 1,2,3-triazol-5-yl)carbamate

484.0 1H NMR (400 MHz, Methanol-d4) δ 8.77 (s, 1H), 8.39-7.53 (m, 4H),5.94 (s, 1H), 3.99 (s, 3H), 1.56 (ddt, J = 72.3, 9.9, 4.5 Hz, 5H), 1.13(dt, J = 9.0, 4.5 Hz, 1H), 0.94 (td, J = 8.2, 4.8 Hz, 1H), 0.84-0.71 (m,1H), 0.57-0.36 (m, 2H), 0.22 (d, J =4.9 Hz, 2H). Compound 268(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-((1R,2S)-[1,1′-bi(cyclopropane)]-2-carboxamido)pyridin-2-yl)-1-methyl-1H- 1,2,3-triazol-5-yl)carbamate

484.0 1H NMR (400 MHz, Methanol-d4) δ 8.78 (s, 1H), 8.26-7.62 (m, 4H),5.94 (d, J = 6.1 Hz, 1H), 3.99 (s, 3H), 1.86-1.41 (m, 5H), 1.14 (dt, J =9.0, 4.5 Hz, 1H), 0.94 (td, J = 8.2, 4.9 Hz, 1H), 0.85-0.72 (m, 1H),0.63-0.37 (m, 2H), 0.21 (d, J = 5.0 Hz, 2H). Compound 269(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4- (5-((1R,2R)-1-cyano-2-fluorocyclopropane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

487.0 1H NMR (400 MHz, Methanol-d4) δ 8.68 (d, J = 89.1 Hz, 1H),8.23-7.57 (m, 4H), 5.95 (d, J = 6.7 Hz, 1H), 5.26 (ddd, J = 62.8, 5.8,4.4 Hz, 1H), 4.00 (d, J = 3.9 Hz, 3H), 2.32-2.12 (m, 2H), 1.62 (s, 4H).Compound 270 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-((1S,2S)-1-cyano-2- fluorocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl-1H- 1,2,3-triazol-5-yl)carbamate

487.0 1H NMR (400 MHz, Methanol-d4) δ 8.79 (s, 1H), 8.22-7.61 (m, 3H),5.95 (s, 1H), 5.26 (ddd, J = 62.8, 5.9, 4.3 Hz, 1H), 4.00 (s, 3H),2.32-2.07 (m, 2H), 1.62 (s, 3H). Compound 271(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4- (5-(6-(1-cyanocyclopropyl)nicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5- yl)carbamate

546.0 1H NMR (400 MHz, Methanol-d4) δ 9.04 (dd, J = 2.4, 0.9 Hz, 1H),8.94 (s, 1H), 8.35 (dd, J = 8.3, 2.3 Hz, 1H), 8.23 (dd, J = 8.7, 2.6 Hz,1H), 8.02 (s, 1H), 7.98-7.90 (m, 1H), 7.92- 7.75 (m, 2H), 5.94 (d, J =6.9 Hz, 1H), 3.99 (s, 3H), 1.97- 1.88 (m, 2H), 1.85 (p, J = 6.4, 5.9 Hz,2H), 1.60 (s, 3H). Compound 272 (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4- (5-(6-(1,1- difluoroethyl)nicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

545.0 1H NMR (400 MHz, Methanol-d4) δ 9.18 (dd, J = 2.2, 0.9 Hz, 1H),8.96 (s, 1H), 8.48 (dd, J = 8.2, 2.3 Hz, 1H), 8.25 (dd, J = 8.7, 2.6 Hz,1H), 8.03 (s, 1H), 7.97 (dd, J = 8.6, 0.8 Hz, 1H), 7.93-7.69 (m, 2H),5.94 (d, J = 7.1 Hz, 1H), 3.99 (s, 3H), 2.04 (t, J = 18.7 Hz, 3H), 1.61(s, 3H). Compound 273 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (1-methyl-4-(5-(2- (methylsulfonyl)isonicotinamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

559.0 1H NMR (400 MHz, Methanol-d4) δ 8.97 (dd, J = 5.0, 0.8 Hz, 1H),8.60 (dd, J = 1.7, 0.8 Hz, 1H), 8.27 (dd, J = 8.7, 2.6 Hz, 1H), 8.20(dd, J = 5.0, 1.7 Hz, 1H), 8.03 (s, 1H), 8.00-7.75 (m, 2H), 5.94 (d, J =7.0 Hz, 1H), 3.99 (s, 3H), 3.30 (s, 3H), 1.61 (s, 3H). Compound 274(R)-1-(2,5-difluoropyridin-3-yl)ethyl (1- methyl-4-(5-(1-methyl-1H-benzo[d]imidazole-6- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

534.0 1H NMR (400 MHz, Methanol-d4) δ 8.99 (s, 1H), 8.32 (s, 1H), 8.27(dd, J = 8.8, 2.3 Hz, 2H), 8.02 (s, 1H), 7.99-7.83 (m, 3H), 7.80 (d, J =8.5 Hz, 1H), 5.95 (d, J = 7.1 Hz, 1H), 4.01 (s, 3H), 3.99 (s, 3H), 1.61(s, 3H). Compound 275 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-(2-fluoro-5- (trifluoromethyl)nicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5- yl)carbamate

567.0 1H NMR (400 MHz, Methanol-d4) δ 8.89 (s, 1H), 8.78 (d, J = 2.3 Hz,1H), 8.66 (dd, J = 8.1, 2.5 Hz, 1H), 8.23 (dd, J = 8.6, 2.6 Hz, 1H),8.03 (s, 1H), 8.00- 7.68 (m, 2H), 5.94 (d, J = 7.1 Hz, 1H), 3.99 (s,3H), 1.61 (s, 3H). Compound 276 (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4- (5-(3,4-dimethylisoxazole-5- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

499.0 1H NMR (400 MHz, DMSO-d6) δ 10.93 (s, 1H), 9.82 (bs, 1H), 8.90 (s,1H), 8.33-7.80 (m, 4H), 5.80 (bs, 1H), 3.89 (s, 3H), 2.29 (s, 3H), 2.25(s, 3H), 1.58 (bs, 3H). Compound 277(R)-1-(2,5-difluoropyridin-3-yl)ethyl (1-methyl-4-(5-(2-methyl-3H-imidazo[4,5-b]pyridine-6-carboxamido)pyridin-2-yl)- 1H-1,2,3-triazol-5-yl)carbamate

535.0 1H NMR (400 MHz, Methanol-d4) δ 8.97 (s, 1H), 8.95 (d, J = 2.0 Hz,1H), 8.49 (d, J = 2.0 Hz, 1H), 8.26 (dd, J = 8.6, 2.6 Hz, 1H), 8.03 (s,1H), 8.00- 7.77 (m, 2H), 5.95 (s, 1H), 3.99 (s, 3H), 2.68 (s, 3H), 1.61(s, 3H). Compound 278 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (1-methyl-4-(5-(1-methyl-1H-pyrazolo[4,3-b]pyridine-6-carboxamido)pyridin-2-yl)- 1H-1,2,3-triazol-5-yl)carbamate

535.0 1H NMR (400 MHz, DMSO-d6) δ 10.80 (s, 1H), 9.81 (s, 1H), 9.08 (d,J = 1.9 Hz, 1H), 8.93 (s, 1H), 8.77 (t, J = 1.4 Hz, 1H), 8.42 (d, J =1.0 Hz, 1H), 8.33-8.12 (m, 2H), 8.08-7.87 (m, 2H), 5.81 (s, 1H), 4.20(s, 3H), 3.88 (s, 3H), 1.54 (s, 3H). Compound 279(R)-1-(2,5-difluoropyridin-3-yl)ethyl (1-methyl-4-(5-(3-methylbenzo[d]isoxazole-6-carboxamido)pyridin-2-yl)-1H-1,2,3- triazol-5-yl)carbamate

535.0 1H NMR (400 MHz, Methanol-d4) δ 8.98 (s, 1H), 8.26 (dd, J = 8.6,2.6 Hz, 1H), 8.21 (t, J = 1.0 Hz, 1H), 8.02 (s, 1H), 8.00-7.80 (m, 4H),5.95 (d, J = 6.9 Hz, 1H), 3.99 (s, 3H), 2.64 (s, 3H), 1.61 (s, 3H).Compound 280 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-(2-cyclopropyloxazole-5- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

511.0 1H NMR (400 MHz, DMSO-d6) δ 10.47 (bs, 1H), 9.80 (bs, 1H), 8.84(s, 1H), 8.34-8.09 (m, 2H), 8.09- 7.65 (m, 3H), 5.79 (bs, 1H), 3.88 (s,3H), 2.30-2.18 (m, 1H), 1.53 (bs, 3H), 1.21- 1.00 (m, 4H). Compound 281(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4- (5-(3-methoxyisoxazole-5-carboxamido)pyridin-2-yl)-1-methyl-1H- 1,2,3-triazol-5-yl)carbamate

501.0 1H NMR (400 MHz, DMSO-d6) δ 10.97 (bs, 1H), 9.82 (bs, 1H), 8.87(s, 1H), 8.36-7.65 (m, 4H), 7.06 (s, 1H), 5.80 (bs, 1H), 3.99 (s, 3H),3.89 (s, 3H), 1.54 (bs, 3H). Compound 282(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-(2-(dimethylamino)pyrimidine-5-carboxamido)pyridin-2-yl)-1-methyl-1H- 1,2,3-triazol-5-yl)carbamate

524.9 1H NMR (400 MHz, Methanol-d4) δ 8.90 (s, 2H), 8.19 (dd, J = 8.6,2.6 Hz, 1H), 8.10-7.99 (m, 2H), 7.97-7.69 (m, 2H), 5.94 (d, J = 7.1 Hz,1H), 3.98 (s, 3H), 3.28 (s, 6H), 1.60 (s, 3H). Compound 283(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4- (5-(2-cyclopropylpyrimidine-5-carboxamido)pyridin-2-yl)-1-methyl-1H- 1,2,3-triazol-5-yl)carbamate

522.0 1H NMR (400 MHz, Methanol-d4) δ 9.12 (s, 2H), 8.93 (s, 1H), 8.23(dd, J = 8.6, 2.6 Hz, 1H), 8.02 (s, 1H), 7.99-7.76 (m, 2H), 5.94 (d, J =7.1 Hz, 1H), 3.99 (s, 3H), 2.42-2.26 (m, 1H), 1.61 (s, 3H), 1.22 (tt, J= 8.1, 2.9 Hz, 4H). Compound 284 (R)-1-(2,5-difluoropyridin-3-yl)ethyl(1- methyl-4-(5-(2-morpholinopyrimidine-5-carboxamido)pyridin-2-yl)-1H-1,2,3- triazol-5-yl)carbamate

567.0 1H NMR (400 MHz, Methanol-d4) δ 8.92 (s, 2H), 8.19 (dd, J = 8.7,2.6 Hz, 1H), 8.09-7.99 (m, 2H), 7.98-7.76 (m, 2H), 5.94 (d, J = 6.8 Hz,1H), 3.99 (s, 3H), 3.94 (dd, J = 5.6, 4.2 Hz, 4H), 3.80-3.71 (m, 4H),1.61 (s, 3H). Compound 285 (R)-1-(2-chloro-5-fluoropyridin-3- yl)ethyl(4-(5-((1RS,2RS)-2- cyanocyclopropane-1-carboxamido)pyridin-2-yl)-1-methyl-1H- 1,2,3-triazol-5-yl)carbamate

485.1 1H NMR (400 MHz, Methanol-d4) δ 9.13-8.76 (m, 1H), 8.43-8.07 (m,2H), 7.93 (m, 2H), 6.03 (m 1H), 4.01 (s, 3H), 2.48 (m, 1H), 2.12 (m,1H), 1.84- 1.32 (m, 5H). Compound 288 (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl (1-methyl-4-(5-(6- (trifluoromethyl)nicotinamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

565.0 1H NMR (400 MHz, Methanol-d4) δ 9.26 (d, J = 2.1 Hz, 1H), 8.97 (s,1H), 8.64-8.52 (m, 1H), 8.34- 8.15 (m, 2H), 8.11-7.68 (m, 3H), 6.03 (d,J = 7.2 Hz, 1H), 4.00 (s, 3H), 1.60 (s, 3H). Compound 289(R)-1-(2-chloro-5-fluoropyridin-3- yl)ethyl (4-(5-(2-(difluoromethyl)pyrimidine-5- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

548.0 1H NMR (400 MHz, Methanol-d4) δ 9.42 (s, 2H), 8.97 (s, 1H), 8.24(dd, J = 8.7, 2.6 Hz, 2H), 8.03-7.71 (m, 2H), 6.84 (t, J = 54.2 Hz, 1H),6.03 (s, 1H), 3.99 (s, 3H), 1.60 (s, 3H). Compound 290(R)-1-(2-chloro-5-fluoropyridin-3- yl)ethyl (1-methyl-4-(5-(2-(trifluoromethyl)pyrimidine-5- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

566.0 1H NMR (400 MHz, Methanol-d4) δ 9.47 (s, 2H), 8.97 (s, 1H),8.37-8.14 (m, 2H), 8.05-7.66 (m, 2H), 6.03 (d, J = 7.0 Hz, 1H), 4.00 (s,3H), 1.60 (s, 3H). Compound 291 (R)-1-(2-fluoropyridin-3-yl)ethyl (4-(5-(3,3-difluoro-1-methylcyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H- 1,2,3-triazol-5-yl)carbamate

490.1 1H NMR (400 MHz, Methanol-d4) δ 8.96 (m, 1H), 8.34-7.99 (m, 3H),7.93 (m, 1H), 7.39 (s, 1H), 6.00 (m, 1H), 4.00 (s, 3H), 3.25-3.05 (m,2H), 2.68- 2.45 (m, 2H), 1.65 (s, 6H). Compound 292(R)-1-(2-fluoropyridin-3-yl)ethyl (4-(5-(6-chloronicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

496.9 1H NMR (400 MHz, Methanol-d4) δ 8.96 (dd, J = 2.6, 0.7 Hz, 2H),8.36 (dd, J = 8.4, 2.6 Hz, 1H), 8.21 (dd, J = 8.6, 2.6 Hz, 1H), 8.16-8.06 (m, 2H), 7.99-7.90 (m, 1H), 7.64 (dd, J = 8.3, 0.7 Hz, 1H), 7.36(s, 1H), 5.99 (d, J = 6.8 Hz, 1H), 3.98 (s, 3H), 1.61 (s, 3H). Compound293 (R)-1-(2-fluoropyridin-3-yl)ethyl (4-(5-(2-chloroisonicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

497.0 1H NMR (400 MHz, Methanol-d4) δ 8.99 (s, 1H), 8.61 (dd, J = 5.1,0.8 Hz, 1H), 8.24 (dd, J = 8.6, 2.6 Hz, 1H), 8.18-8.11 (m, 2H),8.05-7.95 (m, 2H), 7.89 (dd, J = 5.1, 1.5 Hz, 1H), 7.38 (s, 1H), 6.01(d, J = 7.1 Hz, 1H), 4.00 (s, 3H), 1.63 (s, 3H). Compound 294(R)-1-(2-fluoropyridin-3-yl)ethyl (4-(5-(2,3-difluoroisonicotinamido)pyridin-2- yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

499.0 1H NMR (400 MHz, Methanol-d4) δ 8.91 (s, 1H), 8.27-8.10 (m, 4H),7.97 (dd, J = 8.7, 0.7 Hz, 1H), 7.62 (dd, J = 5.0, 4.1 Hz, 1H), 7.36 (s,1H), 5.99 (d, J = 6.7 Hz, 1H), 3.98 (s, 3H), 1.61 (s, 3H). Compound 295(R)-1-(2-fluoropyridin-3-yl)ethyl (4-(5-(6-(difluoromethyl)nicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5- yl)carbamate

513.0 1H NMR (400 MHz, Methanol-d4) δ 9.21 (d, J = 2.0 Hz, 1H), 8.98 (s,1H), 8.53 (dd, J = 8.1, 2.2 Hz, 1H), 8.23 (dd, J = 8.7, 2.6 Hz, 1H),8.16-8.08 (m, 2H), 7.96 (d, J = 8.6 Hz, 1H), 7.88 (d, J = 8.1 Hz, 1H),7.36 (s, 1H), 6.83 (t, J = 55.0 Hz, 1H), 5.99 (d, J = 6.9 Hz, 1H), 3.98(s, 3H), 1.61 (s, 3H). Compound 296 (R)-1-(2-fluoropyridin-3-yl)ethyl(1- methyl-4-(5-(6- (trifluoromethyl)nicotinamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

531.0 1H NMR (400 MHz, Methanol-d4) δ 9.27 (d, J = 2.1 Hz, 1H), 8.98 (s,1H), 8.58 (dd, J = 8.2, 2.2 Hz, 1H), 8.27-8.19 (m, 1H), 8.17-8.07 (m,2H), 7.99 (dd, J = 16.5, 8.4 Hz, 2H), 7.36 (s, 1H), 5.99 (d, J = 6.6 Hz,1H), 3.98 (s, 3H), 1.61 (s, 3H).

Example 55 Preparation of (R)-1-(2-chloropyridin-3-yl) ethyl(4-(5-((1r,3R)-3-cyano-3-fluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (Compound 185)

To a stirring dichloromethane (1 mL) solution of(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((1s,3S)-3-cyano-3-hydroxycyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 139) (0.04 mmol) at 0° C. was added (diethylamino)sulfurtrifluoride (0.04 mmol). It was slowly warmed up to room temperature andstirred for 12 hours. The mixture was diluted with dichloromethane andwashed with saturated aqueous sodium carbonate solution and brine. Theaqueous layer was extracted with dichloromethane, and the combinedorganic extracts were dried (sodium sulfate), filtered, and concentratedin vacuo to afford the title Compound as yellowish oil. The residue waspurified by reverse-phase HPLC to provide (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-((1r,3R)-3-cyano-3-fluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (Compound 185).(MS (m/z) 499.1 [M+H]⁺). 1H NMR (400 MHz, Methanol-d4) δ 8.92 (s, 1H),8.32 (s, 1H), 8.21-7.78 (m, 3H), 7.39 (d, 1H), 6.21-5.92 (m, 1H),5.01-4.65 (m, 2H), 4.00 (s, 3H), 2.76 (m, 1H), 1.94-1.79 (m, 2H), 1.55(d, 3H).

Example 56 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(1-cyano-3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 186)

To a stirring dichloromethane (1 mL) solution of(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(1-cyano-3-oxocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (20 mg, 0.04 mmol) at 0° C. was added(diethylamino)sulfur trifluoride (30 mg, 0.19 mmol). It was slowlywarmed up to room temperature and stirred for 12 hours. The mixture wasdiluted with dichloromethane and washed with saturated aqueous sodiumcarbonate solution. The mixture was concentrated in vacuo. The residuewas purified by reverse-phase HPLC to provide(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(1-cyano-3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (Compound 186).(MS (m/z) 517.0 [M+H]⁺). ¹H NMR (400 MHz, Methanol-d₄) δ 9.10-8.82 (m,1H), 8.33 (s, 1H), 8.29-8.02 (m, 2H), 7.97 (d, 1H), 7.51 (s, 1H), 6.09(d, 1H), 4.02 (d, 3H), 3.57 (m, 2H), 3.33 (m, 2H), 1.65 (s, 3H).

Example 57 Preparation of (S)-2-fluoro-1-(3-fluorophenyl)ethyl(1-methyl-4-(5-(3-methylureido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate(Compound 187)

The hydrochloride salt of (S)-2-fluoro-1-(3-fluorophenyl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 6B) (0.05 mmol) was dissolved in dichloromethane (1 mL),pyridine (0.2 mL). Triphosgene (0.1 mmol) was added and after 10 minutesa 2M solution of methylamine (0.5 mmol) in THF was added. After 30 min,the reaction was concentrated and dissolved in tetrahydrofuran (2 mL),and 1 M aqueous sodium hydroxide solution (2 mL) and stirred vigorouslyfor 10 minutes. The reaction was quenched with sat. ammonium chloride,and extracted with ethyl acetate (2×10 mL). The combined organics weredried over sodium sulfate, concentrated, and purified by reverse-phaseHPLC to provide (S)-2-fluoro-1-(3-fluorophenyl)ethyl(1-methyl-4-(5-(3-methylureido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate(Compound 187). (MS (m/z) 432.2 [M+H]⁺). ¹H NMR (400 MHz, Methanol-d₄) δ8.81 (s, 1H), 8.02 (dd, J=8.7, 2.4 Hz, 1H), 7.81 (d, J=8.8 Hz, 1H),7.61-6.59 (m, 4H), 6.14-5.62 (m, 1H), 4.78-4.39 (m, 2H), 3.98 (s, 3H),2.80 (s, 3H).

Example 58 Preparation of Compounds 188 to 194

Compounds 188 to 194 were generally synthesized according Scheme C, Step4. For example, (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(azetidine-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 188) was prepared as follows.

(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 5A) (Example 21) (0.07 mmol) was taken up in 0.2 mL DCMand 0.1 mL DMF and treated with triethyl-amine (0.183 mmol)) andphenylchloroformate (0.08 mmol). The reaction was stirred for 15 min andazetidine (0.112 mmol) was added as a solution in THF. After 15 min thereaction was concentrated, then taken up in aqueous MeCN and acidifiedwith TFA. Purified by RP-HPLC to provide(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(azetidine-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamateas the TFA salt (Compound 188). (MS (m/z) 457.1 [M+H]+). 1H NMR (400MHz, Acetonitrile-d3) δ 8.93 (s, 1H), 8.59 (bs, 1H), 8.34 (dd, J=4.8,1.9 Hz, 1H), 8.14 (ddd, J=8.8, 2.6, 1.2 Hz, 1H), 7.97 (d, J=8.8 Hz, 1H),7.39 (d, J=15.7 Hz, 2H), 6.04 (q, J=6.6 Hz, 1H), 4.14-4.05 (m, 4H), 3.96(s, 3H), 2.31 (dq, J=8.2, 7.4 Hz, 2H), 1.59 (d, J=6.6 Hz, 3H).

Compounds 188-194 (Table 3) were similarly prepared according to SchemeC, step 4 by reacting (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,Intermediate 5A (Example 21) with the Reagent listed in Table 3 in placeof azetidine following the general process described for Compound 188.

TABLE 3 Compounds prepared according to Scheme C, Step 4. LCMS CompoundNo. Structure Reagent m/z 1H NMR Compound 188 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(azetidine-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol- 5-yl)carbamate

457.1 1H NMR (400 MHz, Acetonitrile-d3) δ 8.93 (s, 1H), 8.59 (bs, 1H),8.34 (dd, J = 4.8, 1.9 Hz, 1H), 8.14 (ddd, J = 8.8, 2.6, 1.2 Hz, 1H),7.97 (d, J = 8.8 Hz, 1H), 7.39 (d, J = 15.7 Hz, 2H), 6.04 (q, J = 6.6Hz, 1H), 4.14-4.05 (m, 4H), 3.96 (s, 3H), 2.31 (dq, J = 8.2, 7.4 Hz,2H), 1.59 (d, J = 6.6 Hz, 3H). Compound 189 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(3- cyanobicyclo[1.1.1]pentane- 1-carboxamido)-4-fluoropyridin-2-yl)-1- methyl-1H-1,2,3-triazol-5- yl)carbamate

487.1 1H NMR (400 MHz, Acetonitrile-d3) δ 8.90 (d, J = 22.7 Hz, 1H),8.62 (s, 1H), 8.35 (dd, J = 4.8, 1.9 Hz, 1H), 8.19- 8.07 (m, 1H), 7.99(dd, J = 8.8, 2.2 Hz, 1H), 7.92 (s, 1H), 7.68 (d, J = 34.5 Hz, 1H), 7.41(s, 1H), 6.04 (q, J = 6.6 Hz, 1H), 3.96 (s, 3H), 3.71 (dd, J = 5.6, 4.1Hz, 3H), 3.51 (t, J = 4.9 Hz, 4H), 1.95 (s, 0H), 1.59 (d, J = 6.6 Hz,3H). Compound 190 (R)-1-(2-chloropyridin-3- yl)ethyl (1-methyl-4-(5-((R)-3-methylpyrrolidine-1- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5- yl)carbamate

485.1 1H NMR (400 MHz, Acetonitrile-d3) d 9.08 (s, 1H), 8.34 (dd, J =4.8, 1.9 Hz, 1H), 8.24 (dd, J = 8.9, 2.4 Hz, 1H), 7.98 (d, J = 8.9 Hz,1H), 7.54 (s, 1H), 7.42 (s, 2H), 6.03 (q, J = 6.6 Hz, 1H), 3.96 (s, 3H),3.70-3.54 (m, 2H), 2.99 (dd, J = 9.9, 8.1 Hz, 1H), 2.35 (t, J = 7.4 Hz,1H), 2.14-2.05 (m, 1H), 2.09 (s, 1H), 1.68- 1.55 (m, 4H), 1.11 (d, J =6.6 Hz, 3H). Compound 191 (R)-1-(2-chloropyridin-3- yl)ethyl (4-(5-(3-cyanoazetidine-1- carboxamido)pyridin-2-yl)- 1-methyl-1H-1,2,3-triazol-5-yl)carbamate

482.1 1H NMR (400 MHz, Acetonitrile-d3) δ 8.79 (m, 2H), 8.47 (s, 1H),8.15 (d, J = 20.4 Hz, 1H), 8.05 (dd, J = 8.7, 2.4 Hz, 1H), 8.00 (s, 1H),7.06 (s, 1H), 5.90 (q, J = 6.6 Hz, 1H), 3.96 (t, J = 1.0 Hz, 3H), 2.31(s, 3H), 1.78-1.68 (m, 5H), 1.54 (d, J = 6.1 Hz, 3H). Compound 192(R)-1-(2-chloropyridin-3- yl)ethyl (1-methyl-4-(5-((R)-2-methylpyrrolidine-1- carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5- yl)carbamate

485.1 1H NMR (400 MHz, Acetonitrile-d3) δ 9.01 (d, J = 2.4 Hz, 1H), 8.78(s, 1H), 8.34 (dd, J = 4.8, 1.9 Hz, 1H), 8.21 (dd, J = 8.8, 2.5 Hz, 1H),7.98 (d, J = 8.8 Hz, 1H), 7.40 (s, 1H), 6.04 (q, J = 6.6 Hz, 1H), 4.13(pd, J = 6.4, 2.8 Hz, 1H), 3.96 (s, 3H), 3.55 (ddd, J = 9.9, 7.5, 3.6Hz, 1H), 3.50-3.39 (m, 1H), 2.07 (dddd, J = 13.6, 10.9, 5.7, 4.0 Hz,2H), 1.95 (d, J = 1.7 Hz, OH), 1.73-1.61 (m, 1H), 1.59 (d, J = 5.9 Hz,3H), 1.24 (d, J = 6.3 Hz, 3H). Compound 193 (R)-1-(2-chloropyridin-3-yl)ethyl (4-(5-(3,3- difluoropyrrolidine-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol- 5-yl)carbamate

507.1 1H NMR (400 MHz, Acetonitrile-d3) d 8.91 (s, 1H), 8.58 (s, 0H),8.35 (dd, J = 4.7, 1.8 Hz, 1H), 8.15 (dd, J = 8.8, 2.4 Hz, 1H), 7.99 (d,J = 8.8 Hz, 1H), 7.47 (s, 1H), 7.42 (s, 1H), 6.04 (q, J = 6.6 Hz, 1H),,3.96 (s, 3H), 3.86 (t, J = 13.1 Hz, 2H), 3.73 (t, J = 7.4 Hz, 2H), 2.51(tt, J = 14.3, 7.4 Hz, 2H), 1.58 (s, 3H). Compound 194 (R)-1-(2-chloropyridin-3- yl)ethyl (1-methyl-4- (5-(pyrrolidine-1-carboxamido)pyridin- 2-yl)-1H-1,2,3- triazol-5- yl)carbamate

471.1 1H NMR (400 MHz, Acetonitrile-d3) d 9.08 (s, 1H), 8.34 (dd, J =4.8, 1.9 Hz, 1H), 8.24 (dd, J = 8.9, 2.4 Hz, 1H), 7.98 (d, J = 8.9 Hz,1H), 7.54 (s, 1H), 7.42 (s, 2H), 6.03 (q, J = 6.6 Hz, 1H), 3.96 (s, 3H),3.70-3.54 (m, 2H), 2.99 (dd, J = 9.9, 8.1 Hz, 1H), 2.35 (t, J = 7.4 Hz,1H), 2.14-2.05 (m, 1H), 2.09 (s, 1H), 1.68- 1.55 (m, 4H), 1.11 (d, J =6.6 Hz, 3H).

Example 59 Preparation of Compounds 297 to 303

Compounds 297 to 304 were generally synthesized according Scheme C, Step4, followed by protecting group removal. For example,(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(3-cyanoazetidine-3-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 297) was prepared as follows.

Step 1: tert-butyl(R)-3-cyano-3-((6-(5-(((1-(2,5-difluoropyridin-3yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyridin-3-yl)carbamoyl)azetidine-1-carboxylate

A vial was charged with (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (Intermediate 5B) (0.12 mmol),1-(tert-butoxycarbonyl)-3-cyanoazetidine-3-carboxylic acid (0.15 mmol),N-ethyl-N′-(3-dimethylaminopropyl) carbodiimide hydrochloride (0.24mmol) and pyridine (2 mL). The reaction mixture was stirred for 2 hoursat room temperature, concentrated, diluted with water and extracted withEtOAc (3×). The combined organic layers were washed with brine, driedover MgSO₄, filtered and concentrated to provide tert-butyl(R)-3-cyano-3-((6-(5-(((1-(2,5-difluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyridin-3-yl)carbamoyl)azetidine-1-carboxylate,which was used without further purification. (MS (m/z) 584.3 [M+H]⁺).

Step 2: (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(3-cyanoazetidine-3-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

A solution of tert-butyl(R)-3-cyano-3-((6-(5-(((1-(2,5-difluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyridin-3-yl)carbamoyl)azetidine-1-carboxylate(0.12 mmol) in DCM (3 mL) and TFA (1 mL) was stirred at room temperaturefor 1 hour. The reaction was concentrated and purified by reverse phaseHPLC to provide (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(3-cyanoazetidine-3-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamateas the trifluoroacetic acid salt. (MS (m/z) 484.0 [M+H]⁺). 1H NMR (400MHz, DMSO-d6) δ 10.94 (s, 1H), 9.85 (bs, 1H), 9.31 (bs, 2H), 8.69 (bs,1H), 8.20 (bs, 1H), 8.11-7.83 (m, 3H), 5.80 (bs, 1H), 4.53 (q, J=11.4Hz, 4H), 3.90 (s, 3H), 1.41 (bs, 3H).

Compounds 298-303 (Table 4) were similarly prepared according to SchemeC, Step 4 by reacting (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride, (Intermediate 5B) (Example 22) with the Reagent listed inTable 4 in place of1-(tert-butoxycarbonyl)-3-cyanoazetidine-3-carboxylic acid.

TABLE 4 Compounds prepared according to Scheme C, Step 4. LCMS CompoundNo. Structure Reagent m/z 1H NMR Compound 297(R)-1-(2,5-difluoropyridin- 3-yl)ethyl (4-(5-(3- cyanoazetidine-3-carboxamido)pyridin-2-yl)- 1-methyl-1H-1,2,3-triazol- 5-yl)carbamate

484.0 1H NMR (400 MHz, DMSO-d6) δ 10.94 (s, 1H), 9.85 (bs, 1H), 9.31(bs, 2H), 8.69 (bs, 1H), 8.20 (bs, 1H), 8.11- 7.83 (m, 3H), 5.80 (bs,1H), 4.53 (q, J = 11.4 Hz, 4H), 3.90 (s, 3H), 1.41 (bs, 3H). Compound298 (R)-1-(2,5-difluoropyridin- 3-yl)ethyl (4-(5-(3-(difluoromethyl)azetidine- 3-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3- triazol-5-yl)carbamate

509.2 1H NMR (400 MHz, DMSO-d6) δ 10.61 (s, 1H), 9.84 (bs, 1H), 9.20(bs, 1H), 8.87 (bs, 1H), 8.71 (bs, 1H), 8.35- 7.75 (m, 4H), 6.63 (t, J =55.1 Hz, 1H), 5.79 (bs, 1H), 4.51-4.30 (m, 2H), 4.29-4.10 (m, 2H), 3.89(s, 3H), 1.81- 1.07 (bs, 3H). Compound 299 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-(4- cyanopiperidine-4- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol- 5-yl)carbamate

512.1 1H NMR (400 MHz, DMSO-d6) δ 11.95 (bs, 1H), 10.66 (s, 1H), 9.84(bs, 1H), 8.97-8.40 (m, 3H), 8.34-7.89 (m, 3H), 5.79 (bs, 1H), 3.90 (s,3H), 3.56-3.37 (m, 2H), 3.22-3.01 (m, 2H), 2.49-2.39 (m, 2H), 2.37-2.19(m, 2H), 1.58 (bs, 3H). Compound 300 (R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-(1- (aminomethyl)-2,2- difluorocyclopropane-1-carboxamido)pyridin-2-yl)- 1-methyl-1H-1,2,3-triazol- 5-yl)carbamate

509.0 1H NMR (400 MHz, DMSO-d6) δ 10.43 (d, J = 4.4 Hz, 1H), 9.83 (bs,1H), 8.77-8.65 (m, 1H), 8.42-7.80 (m, 5H), 5.80 (bs, 1H), 3.89 (s, 3H),3.79 (dd, J = 14.1, 5.3 Hz, 1H), 3.08 (dd, J = 13.7, 6.1 Hz, 1H), 2.47(m, 1H), 2.24- 2.06 (m, 1H), 1.57 (bs, 3H). Compound 301(R)-1-(2,5-difluoropyridin- 3-yl)ethyl (4-(5-(1- (aminomethyl)-3,3-difluorocyclobutane-1- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol- 5-yl)carbamate

523.0 1H NMR (400 MHz, DMSO-d6) δ 10.26 (s, 1H), 9.82 (bs, 1H), 8.74 (s,1H), 8.32-7.74 (m, 7H), 5.80 (bs, 1H), 3.89 (s, 3H), 3.53-3.34 (m, 2H),3.20 (q, J = 13.3 Hz, 2H), 2.90 (q, J = 12.6 Hz, 2H), 1.56 (bs, 3H).Compound 302 (R)-1-(2,5-difluoropyridin- 3-yl)ethyl (4-(5-(3-cyanopyrrolidine-3- carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol- 5-yl)carbamate

498.0 1H NMR (400 MHz, DMSO-d6) δ 10.90 (s, 1H), 9.84 (bs, 1H), 9.37(bs, 2H), 8.71 (s, 1H), 8.37-7.79 (m, 4H), 5.79 (bs, 1H), 4.00 (d, J =12.6 Hz, 1H), 3.92-3.82 (m, 4H), 3.52-3.41 (m, 1H), 3.42-3.30 (m, 1H),2.75 (t, J = 7.2 Hz, 2H), 1.58 (bs, 3H). Compound 303(R)-1-(2,5-difluoropyridin- 3-yl)ethyl (4-(5-(1-(aminomethyl)cyclobutane- 1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3- triazol-5-yl)carbamate

487.1 1H NMR (400 MHz, DMSO-d6) δ 9.98 (s, 1H), 9.82 (bs, 1H), 8.77 (d,J = 2.4 Hz, 1H), 8.21 (bs, 1H), 8.13 (dd, J = 8.7, 2.5 Hz, 1H), 8.03(bs, 1H), 7.94 (d, J = 8.7 Hz, 1H), 7.85 (bs, 3H), 5.80 (bs, 1H), 3.89(s, 3H), 3.40-3.28 (m, 2H), 2.59-2.52 (m, 2H), 2.18-1.93 (m, 3H),1.93-1.78 (m, 1H), 1.55 (bs, 3H).

Example 60 Preparation of (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-(1-(aminomethyl)-3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 304)

Step 1: (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-(1-(((tert-butoxycarbonyl)amino)methyl)-3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

A vial was charged with (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (Intermediate 5C) (0.19 mmol),1-(((tert-butoxycarbonyl)amino)methyl)-3,3-difluorocyclobutane-1-carboxylicacid (0.25 mmol), N-ethyl-N′-(3-dimethylaminopropyl) carbodiimidehydrochloride (0.38 mmol) and pyridine (2 mL). The reaction mixture wasstirred for 2 hours at RT, concentrated, diluted with water andextracted with EtOAc (3×). The combined organic layers were washed withbrine, dried over MgSO₄, filtered and concentrated to provide(R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-(1-(((tert-butoxycarbonyl)amino)methyl)-3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatewhich was used without further purification. (MS (m/z) 639.1. [M+H]⁺).

Step 2: (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-(1-(aminomethyl)-3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

A solution of (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-(1-(((tert-butoxycarbonyl)amino)methyl)-3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(0.12 mmol) in DCM (3 mL) and TFA (1 mL) was stirred at RT for 18 hours.The reaction was concentrated and purified by reverse phase HPLC toprovide (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-(1-(aminomethyl)-3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamateas the trifluoroacetic acid salt. (MS (m/z) 539.0 [M+H]⁺). 1H NMR (400MHz, DMSO-d6) δ 10.24 (s, 1H), 9.87 (bs, 1H), 8.76 (s, 1H), 8.44 (bs,1H), 8.15-7.68 (m, 5H), 5.84 (bs, 1H), 3.90 (s, 3H), 3.51-3.22 (m, 2H),3.21 (q, J=13.3 Hz, 2H), 2.90 (q, J=13.0 Hz, 2H), 1.57 (bs, 3H).

Example 61 Preparation of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(3-cyano-1-(2,2,2-trifluoroethyl)azetidine-3-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 305)

A vial was charged with (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(3-cyanoazetidine-3-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamateas the trifluoroacetic acid salt (0.03 mmol), triethylamine (0.15 mmol)and ACN (2 mL). 2,2,2-Trifluoroethyl trifluoromethanesulfonate (0.09mmol) was added and the solution was heated at 60° C. for 2 hours. Thereaction was concentrated and purified by reverse phase HPLC to provide(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(3-cyano-1-(2,2,2-trifluoroethyl)azetidine-3-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate.(MS (m/z) 565.9 [M+H]⁺). 1H NMR (400 MHz, DMSO-d6) δ 10.77 (bs, 1H),9.84 (bs, 1H), 8.70 (bs, 1H), 8.19 (bs, 1H), 8.13-7.91 (m, 3H), 5.80(bs, 1H), 3.96 (d, J=7.6 Hz, 2H), 3.93-3.86 (m, 5H), 3.37 (q, J=10.1 Hz,2H), 1.58 (bs, 3H).

Example 62 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(1-methyl-4-(5-((1r,3R)-3-((2,2,2-trifluoroethyl)amino)cyclobutane-1-carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate(Compound 306)

Step 1: (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((1r,3R)-3-((tert-butoxycarbonyl)amino)cyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (0.146 mmol) suspended in dimethylformamide (2 mL) wastreated with(1r,3r)-3-((tert-butoxycarbonyl)amino)cyclobutane-1-carboxylic acid(0.186 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimidehydrochloride (0.438 mmol), and pyridine (0.869 mmol). The reactionmixture was stirred at room temperature for 30 minutes. The reactionmixture was concentrated to give the crude product.

Step 2: (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((1r,3R)-3-aminocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((1r,3R)-3-((tert-butoxycarbonyl)amino)cyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(0.105 mmol) dissolved in dichloromethane (2 mL) was treated withtrifluoroacetic acid (10.5 mmol). The reaction mixture was stirred atroom temperature overnight. The reaction mixture was concentrated. Theresidue was re-dissolved in ethyl acetate and washed with saturatedsodium bicarbonate solution. The layers were separated. The organiclayer was concentrated to give the crude product.

Step 3: (R)-1-(2-chloropyridin-3-yl)ethyl(1-methyl-4-(5-((1r,3R)-3-((2,2,2-trifluoroethyl)amino)cyclobutane-1-carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-((1r,3R)-3-aminocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(0.0425 mmol) dissolved in acetonitrile (4 mL) was treated withtriethylamine (0.215 mmol) followed by 2,2,2-trifluoroethyltrifluoromethanesulfonate (0.144 mmol). The reaction mixture was stirredat room temperature overnight and then concentrated. The residue waspurified by HPLC to give (R)-1-(2-chloropyridin-3-yl)ethyl(1-methyl-4-(5-((1r,3R)-3-((2,2,2-trifluoroethyl)amino)cyclobutane-1-carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate.(MS (m/z) 553.1 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ 8.86 (s, 1H),8.39-8.24 (m, 2H), 8.09 (dd, J=8.5, 2.8 Hz, 1H), 7.90 (d, J=8.8 Hz, 1H),7.45 (dd, J=7.7, 4.8 Hz, 1H), 6.07 (s, 1H), 4.16 (p, J=8.0 Hz, 1H), 3.99(s, 3H), 3.94 (t, J=9.1 Hz, 1H), 2.74 (td, J=8.6, 8.1, 4.1 Hz, 2H), 2.57(dt, J=13.6, 9.3 Hz, 2H), 1.55 (d, J=46.0 Hz, 3H).

Example 63 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(1-methyl-4-(5-((1s,3S)-3-((2,2,2-trifluoroethyl)amino)cyclobutane-1-carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate(Compound 307)

The title compound was prepared similarly to Example 62 using(1s,3s)-3-((tert-butoxycarbonyl)amino)cyclobutane-1-carboxylic acid(0.186 mmol) in place of(1r,3r)-3-((tert-butoxycarbonyl)amino)cyclobutane-1-carboxylic acid. (MS(m/z) 553 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ 8.84 (s, 1H), 8.31(s, 1H), 8.09 (dd, J=8.7, 2.6 Hz, 1H), 7.90 (d, J=8.6 Hz, 1H), 7.46 (s,2H), 6.07 (s, 1H), 3.99 (s, 3H), 3.82-3.69 (m, 2H), 3.11 (d, J=8.5 Hz,2H), 2.74-2.60 (m, 2H), 2.43 (d, J=10.6 Hz, 2H), 1.61 (s, 3H).

Example 64 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(1-methyl-4-(5-((1R,5S,6r)-3-(2,2,2-trifluoroethyl)-3-azabicyclo[3.1.0]hexane-6-carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate(Compound 308)

The title compound was prepared similarly to Example 62 usingexo-3-[(tert-butoxy)carbonyl]-3-azabicyclo[3.1.0]hexane-6-carboxylicacid (0.186 mmol) in place of(1r,3r)-3-((tert-butoxycarbonyl)amino)cyclobutane-1-carboxylic acid. (MS(m/z) 565.1 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ 8.95 (s, 1H), 8.33(s, 1H), 8.13 (d, J=7.8 Hz, 2H), 7.90 (d, J=8.8 Hz, 1H), 7.48 (s, 1H),6.09 (d, J=6.9 Hz, 1H), 4.00 (s, 2H), 3.24 (dt, J=19.5, 9.5 Hz, 4H),2.87-2.76 (m, 2H), 2.21 (t, J=2.9 Hz, 1H), 2.10 (t, J=2.7 Hz, 2H), 1.63(s, 3H).

Example 65 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(1-methyl-4-(5-(1-(2,2,2-trifluoroethyl)azetidine-3-carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate(Compound 309)

The title compound was prepared similarly to Example 62 using 1-(tertbutoxycarbonyl)azetidine-3-carboxylic acid (0.186 mmol) in place of(1r,3r)-3-((tert-butoxycarbonyl)amino)cyclobutane-1-carboxylic acid. (MS(m/z) 539.1 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ 8.90 (s, 1H), 8.33(s, 1H), 8.14 (d, J=9.2 Hz, 1H), 7.92 (d, J=8.4 Hz, 1H), 4.43 (d, J=7.8Hz, 2H), 4.13 (d, J=9.1 Hz, 2H), 4.00 (s, 2H), 3.86 (q, J=8.0 Hz, 1H),1.62 (s, 3H).

Example 66 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(1-amino-3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 310)

Step 1: (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(1-((tert-butoxycarbonyl)amino)-3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

A mixture of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (25 mg, 0.061 mmol),1-((tert-butoxycarbonyl)amino)-3,3-difluorocyclobutane-1-carboxylic acid(31 mg, 0.122 mmol), EDCI (20 mg, 0.1 mmol) in pyridine (1 ml) wasstirred 1 h at room temperature. The residue was purified by prep-HPLCwith Gilson prep HPLC (Gemini column, 30-85% CH₃CN in H₂O with 0.1% TFA)to give an intermediate. MS: 607.15 (M+1).

Step 2: (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(1-amino-3,3-difluorocyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

Above intermediate (20 mg) was treated with 2 mL of 4 N HCl in dioxaneand the mixture was stirred at room temperature overnight. The mixturewas concentrated. The residue was purified by prep-HPLC with Gilson prepHPLC (Gemini column, 30-85% CH₃CN in H₂O with 0.1% TFA) to give theproduct. (MS (m/z) 507 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ 8.89 (s,1H), 8.32 (s, 1H), 8.15 (m, 1H), 7.95 (m, 1H), 7.68-7.25 (m, 2H), 6.08(s, 1H), 4.00 (s, 3H), 3.72 (m, 2H), 3.19 (m, 2H), 1.86-1.40 (m, 3H).

Example 67 Synthesis of(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(3-(cyclopropylamino)cyclobutane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 311)

Step 1. (R)-1-(2-chloropyridin-3-yl)ethyl(1-methyl-4-(5-(3-oxocyclobutane-1-carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-aminopyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (0.0975 mmol) suspended in dimethylformamide (2 mL) wastreated with 3-oxocyclobutane-1-carboxylic acid (0.131 mmol),1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.292mmol), and pyridine (0.621 mmol). The reaction mixture was stirred atroom temperature for 30 min. The reaction mixture was diluted with ethylacetate and washed with water. The layers were separated. The organiclayer was concentrated to give crude (R)-1-(2-chloropyridin-3-yl)ethyl(1-methyl-4-(5-(3-oxocyclobutane-1-carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate.

Step 2. (R)-1-(2-chloropyridin-3-yl)ethyl(1-methyl-4-(5-(3-oxocyclobutane-1-carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

(R)-1-(2-chloropyridin-3-yl)ethyl(1-methyl-4-(5-(3-oxocyclobutane-1-carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate(0.0638 mmol) suspended in dichloromethane (1 mL) was treated withcyclopropanamine (0.144 mmol) and triethylamine (0.215 mmol). Afterstirring at room temperature for 10 min, sodium triacetoxyborohydride(0.330 mmol) was added. The reaction mixture was stirred at roomtemperature for 30 minutes. Trifluoroacetic acid (6.53 mmol) was addedto quench the reaction. The reaction mixture was then concentrated andpurified by HPLC to give (R)-1-(2-chloropyridin-3-yl)ethyl(1-methyl-4-(5-(3-oxocyclobutane-1-carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate.(MS (m/z) 511.2 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ 8.88 (s, 1H),8.32 (s, 1H), 8.20-8.00 (m, 2H), 7.91 (d, J=8.6 Hz, 1H), 7.48 (s, 1H),6.08 (d, J=7.1 Hz, 1H), 4.00 (s, 3H), 3.98-3.91 (m, 1H), 3.29-3.17 (m,1H), 2.75 (ddt, J=15.7, 12.1, 8.4 Hz, 3H), 2.65-2.48 (m, 2H), 1.78-1.37(m, 3H), 0.95 (dtt, J=7.4, 5.2, 2.8 Hz, 2H), 0.92-0.84 (m, 2H).

Example 68 Synthesis of(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(3-acetamidobicyclo[1.1.1]pentane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 312)

Step 1. (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(3-((tert-butoxycarbonyl)amino)bicyclo[1.1.1]pentane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

Prepared according to procedures described in Step 1 of Example 62 using3-((tert-butoxycarbonyl)amino)bicyclo[1.1.1]pentane-1-carboxylic acid(0.186 mmol) in place of(1r,3r)-3-((tert-butoxycarbonyl)amino)cyclobutane-1-carboxylic acid.

Step 2. (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(3-aminobicyclo[1.1.1]pentane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

Prepared according to procedures described in Step 2 of Example 62.

Step 3. (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(3-acetamidobicyclo[1.1.1]pentane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(3-aminobicyclo[1.1.1]pentane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(0.0425 mmol) dissolved in acetonitrile was treated with triethylamine(0.287 mmol) followed by acetic anhydride (0.212 mmol). The reactionmixture was stirred at room temperature for 20 minutes. The reactionmixture was concentrated and purified by HPLC to provide thebis-acylated product. The bis-acylated product was dissolved intetrahydrofuran (2 mL) and treated with 1N sodium hydroxide solution(800 μL). The reaction mixture was stirred at room temperature for 100min. The reaction mixture was concentrated and purified by HPLC to give(R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(3-acetamidobicyclo[1.1.1]pentane-1-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate.(MS (m/z) 525.1 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ 8.93 (s, 1H),8.32 (s, 1H), 8.13 (dd, J=8.6, 2.6 Hz, 1H), 7.92 (d, J=8.8 Hz, 1H), 7.55(s, 2H), 6.08 (d, J=6.4 Hz, 1H), 3.99 (s, 3H), 2.44 (s, 6H), 1.94 (d,J=8.8 Hz, 3H), 1.62 (s, 3H).

Example 69 Preparation of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(1-cyanocyclopropane-1-carboxamido)-6-methylpyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 313)

Step 1: tert-butyl(R)-(6-(5-(((1-(2,5-difluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)-2-methylpyridin-3-yl)carbamate

4-(5-((tert-butoxycarbonyl)amino)-6-methylpyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid (3 mmol), Azidotrimethylsilane (3 mmol), and T3P (50% in THF) (4.5mmol) was dissolved in THF (20 mL). Triethyl amine (6 mmol) was addeddropwise at RT resulting in a clear solution after 5-30 minutes.(R)-1-(2,5-difluoropyridin-3-yl)ethan-1-ol (4.5 mmol) was added and thereaction was heated at 80 C for 2 h. Silica gel was then added and thecrude mixture was concentrated in vacuo and then purified by columnchromatography to afford tert-butyl(R)-(6-(5-(((1-(2,5-difluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)-2-methylpyridin-3-yl)carbamate(2.95 mmol).

Step 2: (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-amino-6-methylpyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrogen chloride

(R)-(6-(5-(((1-(2,5-difluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)-2-methylpyridin-3-yl)carbamate(2.95 mmol) was suspended in 10 mL 4 M hydrochloric acid in dioxanes for1 h. The mixture was then concentrated in vacuo to afford(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-amino-6-methylpyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrogen chloride and was used without further purification.

Step 3: (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(1-cyanocyclopropane-1-carboxamido)-6-methylpyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

To a mixture of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-amino-6-methylpyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrogen chloride (0.127 mmol) in pyridine (1 mL) was added1-cyanocyclopropane-1-carboxylic acid (0.254 mmol) andN-Ethyl-N′-(3-dimethylaminopropyl) carbodiimide hydrochloride (0.139mmol). The reaction mixture was left with magnetic stirring for 2 hoursat which point water (1 mL) was added the crude mixture was purified byHPLC to provide (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(1-cyanocyclopropane-1-carboxamido)-6-methylpyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate.(MS (m/z) 483 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ 8.17-7.66 (m,4H), 5.95 (s, 1H), 3.99 (s, 3H), 2.46 (s, 3H), 1.82-1.39 (m, 7H).

Example 70 Preparation of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(1-methyl-4-(6-methyl-5-(2-(trifluoromethyl)pyrimidine-5-carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate(Compound 314)

Step 1: (R)-1-(2,5-difluoropyridin-3-yl)ethyl(1-methyl-4-(6-methyl-5-(2-(trifluoromethyl)pyrimidine-5-carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

To a mixture of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-amino-6-methylpyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (0.127 mmol) in pyridine (0.5 mL) was added2-(trifluoromethyl)pyrimidine-5-carboxylic acid (0.254 mmol) andN-Ethyl-N′-(3-dimethylaminopropyl) carbodiimide hydrochloride (0.139mmol). The reaction mixture was left with magnetic stirring for 2 hoursat which point water (1 mL) was added the crude mixture was purified byHPLC to provide (R)-1-(2,5-difluoropyridin-3-yl)ethyl(1-methyl-4-(6-methyl-5-(2-(trifluoromethyl)pyrimidine-5-carboxamido)pyridin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate.LCMS (MS (m/z) 564 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ 9.47 (s,2H), 8.22-7.60 (m, 4H), 5.97 (s, 1H), 4.01 (s, 3H), 2.53 (s, 3H), 1.58(d, J=27.1 Hz, 3H).

Example 71 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(6-fluoro-5-(6-(trifluoromethyl)nicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 315)

Step 1: (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-amino-6-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

To a solution of (R)-1-(2-chloropyridin-3-yl)ethyl(4-bromo-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (1.4 mmol) intetrahydrofuran (15 mL) at −78° C. was added a 1M solution of lithiumbis(trimethylsilyl)amide (1.4 mmol). After 15 minutes, a 2.5 M solutionof n-butyllithium (3.5 mmol) was added. After 1 hour, a 2 M solution ofzinc chloride (3.5 mmol) was added, and the reaction was stirred at 15°C. for 30 minutes. At this point 6-bromo-2-fluoropyridin-3-amine (1.7mmol) and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)(0.14 mmol) were added to the reaction and the reaction mixture washeated to 80° C. for 3 hours. After completion of the reaction, themixture was cooled and quenched with sat. NaHCO₃, and extracted withethyl acetate (30 mL, ×2). The organics were separated, dried oversodium sulfate, and filtered through a plug of silica and used in thenext step without further purification.

Step 2: (R)-1-(2-chloropyridin-3-yl)ethyl(4-(6-fluoro-5-(6-(trifluoromethyl)nicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

To a mixture of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-amino-6-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(0.15 mmol) in pyridine (1 mL) was added 6-(trifluoromethyl)nicotinicacid (0.3 mmol) and N-ethyl-N′-(3-dimethylaminopropyl) carbodiimidehydrochloride (0.3 mmol). The reaction mixture was left with magneticstirring for 2 hours at which point water (1 mL) was added the crudemixture was purified by HPLC to provide(R)-1-(2-chloropyridin-3-yl)ethyl(4-(6-fluoro-5-(6-(trifluoromethyl)nicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 315). (MS (m/z) 565 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ9.31-9.13 (m, 1H), 8.67-8.43 (m, 2H), 8.43-8.06 (m, 2H), 8.07-7.80 (m,2H), 7.49 (s, 1H), 6.12 (q, J=6.6 Hz, 1H), 4.00 (s, 3H), 1.55 (s, 3H).

Example 72 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(1-cyanocyclopropane-1-carboxamido)-6-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 316)

To a mixture of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-amino-6-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(0.15 mmol) in pyridine (1 mL) was added1-cyanocyclopropane-1-carboxylic acid (0.3 mmol) andN-ethyl-N′-(3-dimethylaminopropyl) carbodiimide hydrochloride (0.3mmol). The reaction mixture was left with magnetic stirring for 2 hoursat which point water (1 mL) was added the crude mixture was purified byHPLC to provide (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(1-cyanocyclopropane-1-carboxamido)-6-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate.(MS (m/z) 485 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ 8.49-8.24 (m,2H), 8.24-8.04 (m, 1H), 7.93 (d, J=8.5 Hz, 1H), 7.68-7.26 (m, 1H), 6.11(q, J=6.7 Hz, 1H), 3.98 (s, 3H), 1.92-1.50 (m, 7H).

Example 73 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(4-fluoro-5-(6-(trifluoromethyl)nicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 317)

Step 1: (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-amino-4-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

To a solution of (R)-1-(2-chloropyridin-3-yl)ethyl(4-bromo-1-methyl-1H-1,2,3-triazol-5-yl)carbamate (1.4 mmol) intetrahydrofuran (15 mL) at −78° C. was added a 1M solution of lithiumbis(trimethylsilyl)amide (1.4 mmol). After 15 minutes, a 2.5 M solutionof n-butyllithium (3.5 mmol) was added. After 1 hour, a 2 M solution ofzinc chloride (3.5 mmol) was added, and the reaction was stirred at 15°C. for 30 minutes. At this point 6-bromo-4-fluoropyridin-3-amine (1.7mmol) and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)(0.14 mmol) were added to the reaction and the reaction mixture washeated to 80° C. for 3 hours. After completion of the reaction, themixture was cooled and quenched with sat. NaHCO₃, and extracted withethyl acetate (30 mL, ×2). The organics were separated, dried oversodium sulfate, and filtered through a plug of silica and used in thenext step without further purification.

Step 2: (R)-1-(2-chloropyridin-3-yl)ethyl(4-(4-fluoro-5-(6-(trifluoromethyl)nicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

To a mixture of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-amino-6-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(0.15 mmol) in pyridine (1 mL) was added 6-(trifluoromethyl)nicotinicacid (0.3 mmol) and N-Ethyl-N′-(3-dimethylaminopropyl) carbodiimidehydrochloride (0.3 mmol). The reaction mixture was left with magneticstirring for 2 hours at which point water (1 mL) was added the crudemixture was purified by HPLC to provide(R)-1-(2-chloropyridin-3-yl)ethyl(4-(4-fluoro-5-(6-(trifluoromethyl)nicotinamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate.(MS (m/z) 564.9 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ 9.38-9.20 (m,1H), 8.60 (d, J=8.1 Hz, 1H), 8.35-8.26 (m, 1H), 8.07-7.93 (m, 2H), 7.88(d, J=11.3 Hz, 1H), 7.63-7.34 (m, 2H), 6.16-6.03 (m, 1H), 4.01 (s, 3H),1.55 (s, 3H).

Example 74 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(6-fluoro-5-(2-(trifluoromethyl)pyrimidine-5-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 318)

To a mixture of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-amino-6-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(0.15 mmol) in pyridine (1 mL) was added2-(trifluoromethyl)pyrimidine-5-carboxylic acid (0.3 mmol) andN-Ethyl-N′-(3-dimethylaminopropyl) carbodiimide hydrochloride (0.3mmol). The reaction mixture was left with magnetic stirring for 2 hoursat which point water (1 mL) was added the crude mixture was purified byHPLC to provide (R)-1-(2-chloropyridin-3-yl)ethyl(4-(6-fluoro-5-(2-(trifluoromethyl)pyrimidine-5-carboxamido)pyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(MS (m/z) 566 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ 9.46 (s, 2H),8.57 (dd, J=9.8, 8.2 Hz, 1H), 8.45-8.02 (m, 2H), 7.98 (d, J=8.2 Hz, 1H),7.49 (s, 1H), 6.12 (q, J=6.5 Hz, 1H), 4.00 (s, 3H), 1.66 (s, 3H).

Example 75 Preparation of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(6-chloronicotinamido)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 319)

Step 1: tert-butyl (2-bromopyrimidin-5-yl)carbamate

To a solution of 2-bromopyrimidin-5-amine (23 mmol) in THF (28 mL) wasadded di-tert-butyl dicarbonate (34.4 mmol). The reaction was heated to70° C. for 16 h, followed by addition of di-tert-butyl dicarbonate (18.3mmol). The reaction was then stirred at 70° C. for 2 h. The reactionmixture was concentrated to provide tert-butyl(2-bromopyrimidin-5-yl)carbamate.

Step 2:4-(5-((tert-butoxycarbonyl)amino)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid (Intermediate 9)

To a solution of 4-bromo-1-methyl-1H-1,2,3-triazole-5-carboxylic acid(48.5 mmol) in tetrahydrofuran (500 mL) at −70° C. was added a 1Msolution of lithium bis(trimethylsilyl)amide (53.4 mmol). After 15minutes, a 2.5 M solution of n-butyllithium (101.8 mmol) was added.After 1 hour, a 2 M solution of zinc chloride (101.9 mmol) was added,and the reaction was stirred at 15° C. for 30 minutes. At this pointtert-butyl (2-bromopyrimidin-5-yl)carbamate (29.1 mmol) and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (4.85 mmol)were added to the reaction and the reaction mixture was heated to 90° C.for 16 h. After completion of the reaction, the mixture was cooled andaqueous 2M sodium hydroxide (800 mL) was added. The organics wereseparated, and aqueous layer was extracted with methyl tert-butyl ether(500 mL×2). The organics were discarded, and the aqueous layer wastreated with 12M HCl (140 mL) and petroleum ether (160 mL). The productcrashed out and was filtered and washed with 30:1 methyl tert-butylether/dichloromethane (70 mL), then purified by column chromatography,providing4-(5-((tert-butoxycarbonyl)amino)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid (Intermediate 9).

Step 3: tert-butyl(R)-(2-(5-(((1-(2,5-difluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyrimidin-5-yl)carbamate

4-(5-((tert-butoxycarbonyl)amino)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid (Intermediate 9) (0.97 mmol), Azidotrimethylsilane (1.46 mmol), andT3P (50% in DMF) (1.46 mmol) was dissolved in THF (5 mL). Triethylamine(1.95 mmol) was added dropwise at room temperature. The reaction washeated to 70° C. for 50 minutes before(R)-1-(2,5-difluoropyridin-3-yl)ethan-1-ol (1.45 mmol) was added and thereaction was heated at 70° C. for another 6 hours. The reaction wasconcentrated and then purified by column chromatography to providetert-butyl(R)-(2-(5-(((1-(2,5-difluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyrimidin-5-yl)carbamate.

Step 4: (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

To a solution of tert-butyl(R)-(2-(5-(((1-(2,5-difluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyrimidin-5-yl)carbamate(0.52 mmol) in dichloromethane (3.4 mL) was added a 4M solution of HClin 1,4-dioxane (3.8 mL). The reaction was stirred for 2 h at roomtemperature. The reaction was concentrated to provide(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate asthe hydrochloride salt.

Step 5: (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(6-chloronicotinamido)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

To a mixture of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (0.073 mmol) in pyridine (1 mL) was added6-chloronicotinic acid (0.082 mmol) andN-Ethyl-N′-(3-dimethylaminopropyl) carbodiimide hydrochloride (0.087mmol). The reaction mixture was stirred for 1 hour then concentrated.The residue was taken up in acetonitrile and water (2 mL) and purifiedby HPLC to provide (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(6-chloronicotinamido)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 319). (MS (m/z) 516.0 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ9.19 (s, 2H), 8.98 (d, J=2.5 Hz, 1H), 8.37 (dd, J=8.3, 2.5 Hz, 1H), 8.04(s, 1H), 7.71-7.59 (m, 2H), 5.96 (d, J=6.2 Hz, 1H), 4.01 (s, 3H), 1.61(s, 3H).

Example 76 Preparation of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(6-chloronicotinamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 320)

Step 1: tert-butyl (5-bromopyrazin-2-yl)carbamate

To a solution of 5-bromopyrazin-2-amine (689 mmol) in DCM (840 mL) wasadded diisopropylethylamine (2.07 mol), DMAP (689 mmol), anddi-tert-butyl dicarbonate (34.4 mmol) at 0° C. The reaction was stirredat room temperature for 16 hours. The reaction mixture was concentrated,then purified by column chromatography to provide tert-butyl(5-bromopyrazin-2-yl)carbamate.

Step 2:4-(5-((tert-butoxycarbonyl)amino)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid

To a solution of 4-bromo-1-methyl-1H-1,2,3-triazole-5-carboxylic acid(242 mmol) in tetrahydrofuran (2.5 L) at −70° C. was added a 1M solutionof lithium bis(trimethylsilyl)amide (266 mmol). After 15 minutes, a 2.5M solution of n-butyllithium (507.5 mmol) was added. After 1 hour, a 2 Msolution of zinc chloride (509.7 mmol) was added, and the reaction wasstirred at 15° C. for 30 minutes. At this point tert-butyl(5-bromopyrazin-2-yl)carbamate (218 mmol) and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (24.2 mmol)were added to the reaction and the reaction mixture was heated to 90° C.for 16 h. After completion of the reaction, the mixture was cooled andaqueous 2M sodium hydroxide (1.5 L) was added. The organics wereseparated, and aqueous layer was extracted with methyl tert-butyl ether(2.0 L×2). The organics were discarded, and the aqueous layer wastreated with 12M HCl (250 mL) and methyl tert-butyl ether (900 mL). Theproduct crashed out and was filtered and washed with methyl tert-butylether (300 mL), providing4-(5-((tert-butoxycarbonyl)amino)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid.

Step 3: tert-butyl(R)-(5-(5-(((1-(2,5-difluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyrazin-2-yl)carbamate

4-(5-((tert-butoxycarbonyl)amino)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid (0.62 mmol), Azidotrimethylsilane (0.94 mmol), and T3P (50% in DMF)(0.94 mmol) was dissolved in THF (5 mL). Triethylamine (1.25 mmol) wasadded dropwise at room temperature, followed by(R)-1-(2,5-difluoropyridin-3-yl)ethan-1-ol (0.93 mmol). The reaction washeated at 70° C. for 6 hours. The reaction was concentrated and thenpurified by column chromatography to provide tert-butyl(R)-(5-(5-(((1-(2,5-difluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyrazin-2-yl)carbamate.

Step 4: (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 10)

To a solution of tert-butyl(R)-(5-(5-(((1-(2,5-difluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)pyrazin-2-yl)carbamate(0.52 mmol) in dichloromethane (3.4 mL) was added a 4M solution of HClin 1,4-dioxane (3.8 mL). The reaction was stirred for 2 h at roomtemperature. The reaction was concentrated to provide(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate as thehydrochloride salt (Intermediate 10).

Step 5: (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(6-chloronicotinamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

To a mixture of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (Intermediate 10) (0.073 mmol) in pyridine (1 mL) wasadded 6-chloronicotinic acid (0.082 mmol) andN-Ethyl-N′-(3-dimethylaminopropyl) carbodiimide hydrochloride (0.087mmol). The reaction mixture was stirred for 1 h then concentrated. Theresidue was taken up in acetonitrile and water (2 mL) and purified byHPLC to provide (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(6-chloronicotinamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 320). (MS (m/z) 515.9 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ9.44 (s, 1H), 9.01-8.90 (m, 2H), 8.38 (dd, J=8.4, 2.5 Hz, 1H), 8.09-7.98(m, 2H), 7.64 (dd, J=8.3, 0.7 Hz, 1H), 5.95 (d, J=7.0 Hz, 1H), 4.00 (s,3H), 1.62 (s, 3H).

Example 77 Preparation of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(6-(difluoromethyl)nicotinamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 321)

Following the procedure described in Example 76 for the preparation of(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(6-chloronicotinamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,using 6-(difluoromethyl)nicotinic acid (0.08 mmol) in place of6-chloronicotinic acid, (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(6-(difluoromethyl)nicotinamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatewas obtained (Compound 321). (MS (m/z) 532.0 [M+H]+). 1H NMR (400 MHz,Methanol-d4) δ 9.46 (d, J=1.5 Hz, 1H), 9.29-9.16 (m, 1H), 8.97 (d, J=1.6Hz, 1H), 8.55 (dd, J=8.2, 2.2 Hz, 1H), 8.05 (s, 1H), 7.93-7.78 (m, 2H),6.83 (t, J=55.0 Hz, 1H), 5.95 (d, J=6.8 Hz, 1H), 4.00 (s, 3H), 1.62 (s,3H).

Example 78 Preparation of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(1-methyl-4-(5-(6-(trifluoromethyl)nicotinamido)pyrazin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate(Compound 322)

Following the procedure described in Example 76 for the preparation of(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(6-chloronicotinamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,using 6-(trifluoromethyl)nicotinic acid (0.08 mmol) in place of6-chloronicotinic acid, (R)-1-(2,5-difluoropyridin-3-yl)ethyl(1-methyl-4-(5-(6-(trifluoromethyl)nicotinamido)pyrazin-2-yl)-1H-1,2,3-triazol-5-yl)carbamatewas obtained (Compound 322). (MS (m/z) 549.9 [M+H]+). 1H NMR (400 MHz,Methanol-d4) δ 9.49 (d, J=20.4 Hz, 1H), 9.27 (d, J=2.1 Hz, 1H), 8.98 (d,J=1.5 Hz, 1H), 8.70-8.50 (m, 1H), 8.11-7.70 (m, 3H), 5.95 (d, J=6.9 Hz,1H), 4.00 (s, 3H), 1.63 (s, 3H).

Example 79 Preparation of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(2,3-difluoroisonicotinamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 323)

Following the procedure described in Example 76 for the preparation of(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(6-chloronicotinamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,using 2,3-difluoroisonicotinic acid (0.08 mmol) in place of6-chloronicotinic acid, (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(2,3-difluoroisonicotinamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatewas obtained (Compound 323). (MS (m/z) 518.0 [M+H]+). 1H NMR (400 MHz,Methanol-d4) δ 9.41 (s, 1H), 8.96 (d, J=1.5 Hz, 1H), 8.14 (dd, J=5.1,1.4 Hz, 1H), 8.05 (s, 1H), 8.00-7.72 (m, 1H), 7.62 (dd, J=5.0, 4.0 Hz,1H), 5.95 (q, J=6.6 Hz, 1H), 4.00 (s, 3H), 1.62 (s, 3H).

Example 80 Preparation of (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(2-(difluoromethyl)pyrimidine-5-carboxamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 324)

Following the procedure described in Example 76 for the preparation of(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(6-chloronicotinamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,using (R)-1-(2-chloropyridin-3-yl)ethan-1-ol (4.64 mmol) in place of(R)-1-(2,5-difluoropyridin-3-yl)ethan-1-ol in step 3, and2-(difluoromethyl)pyrimidine-5-carboxylic acid (0.08 mmol) in place of6-chloronicotinic acid in step 5, (R)-1-(2-chloropyridin-3-yl)ethyl(4-(5-(2-(difluoromethyl)pyrimidine-5-carboxamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatewas obtained (Compound 324). (MS (m/z) 531.0 [M+H]+). 1H NMR (400 MHz,Methanol-d4) δ 9.56-9.27 (m, 3H), 8.96 (s, 1H), 8.43-7.85 (m, 2H), 7.52(s, 1H), 6.84 (t, J=54.2 Hz, 1H), 6.07 (t, J=6.5 Hz, 1H), 4.00 (s, 3H),1.61 (s, 3H).

Example 81 Preparation of (R)-1-(2-fluoropyridin-3-yl)ethyl(1-methyl-4-(5-(2-(trifluoromethyl)pyrimidine-5-carboxamido)pyrazin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate(Compound 325)

Following the procedure described in Example 76 for the preparation of(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(6-chloronicotinamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,using (R)-1-(2-fluoropyridin-3-yl)ethan-1-ol (4.64 mmol) in place of(R)-1-(2,5-difluoropyridin-3-yl)ethan-1-ol in step 3, and2-(trifluoromethyl)pyrimidine-5-carboxylic acid (0.08 mmol) in place of6-chloronicotinic acid in step 5, (R)-1-(2-fluoropyridin-3-yl)ethyl(1-methyl-4-(5-(2-(trifluoromethyl)pyrimidine-5-carboxamido)pyrazin-2-yl)-1H-1,2,3-triazol-5-yl)carbamatewas obtained (Compound 325). (MS (m/z) 532.9 [M+H]+). 1H NMR (400 MHz,Methanol-d4) δ 9.49 (s, 2H), 9.45 (s, 1H), 8.97 (d, J=1.6 Hz, 1H),8.23-7.85 (m, 2H), 7.41 (s, 1H), 5.99 (q, J=6.7 Hz, 1H), 3.99 (s, 3H),1.63 (s, 3H).

Example 82 Preparation of (R)-1-(2-fluoropyridin-3-yl)ethyl(1-methyl-4-(5-(6-(trifluoromethyl)nicotinamido)pyrazin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate(Compound 326)

Following the procedure described in Example 76 for the preparation of(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(6-chloronicotinamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,using (R)-1-(2-fluoropyridin-3-yl)ethan-1-ol (4.64 mmol) in place of(R)-1-(2,5-difluoropyridin-3-yl)ethan-1-ol in step 3, and6-(trifluoromethyl)nicotinic acid (0.08 mmol) in place of6-chloronicotinic acid in step 5, (R)-1-(2-fluoropyridin-3-yl)ethyl(1-methyl-4-(5-(6-(trifluoromethyl)nicotinamido)pyrazin-2-yl)-1H-1,2,3-triazol-5-yl)carbamatewas obtained (Compound 326). (MS (m/z) 532.0 [M+H]+). 1H NMR (400 MHz,Methanol-d4) δ 9.47 (s, 1H), 9.28 (d, J=2.1 Hz, 1H), 8.97 (d, J=1.5 Hz,1H), 8.60 (dd, J=8.3, 2.1 Hz, 1H), 8.25-8.06 (m, 2H), 8.01 (dd, J=8.2,0.8 Hz, 1H), 7.41 (s, 1H), 5.99 (q, J=6.6 Hz, 1H), 3.99 (s, 3H), 1.63(s, 3H).

Example 83 Preparation of (R)-1-(2-fluoropyridin-3-yl)ethyl(4-(5-(2-(difluoromethyl)pyrimidine-5-carboxamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 327)

Following the procedure described in Example 76 for the preparation of(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(6-chloronicotinamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate,using (R)-1-(2-fluoropyridin-3-yl)ethan-1-ol (4.64 mmol) in place of(R)-1-(2,5-difluoropyridin-3-yl)ethan-1-ol in step 3, and2-(difluoromethyl)pyrimidine-5-carboxylic acid (0.08 mmol) in place of6-chloronicotinic acid in step 5, (R)-1-(2-fluoropyridin-3-yl)ethyl(4-(5-(2-(difluoromethyl)pyrimidine-5-carboxamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatewas obtained (Compound 327). (MS (m/z) 514.9 [M+H]+). 1H NMR (400 MHz,Methanol-d4) δ 9.62-9.34 (m, 3H), 8.97 (s, 1H), 8.30-7.93 (m, 2H), 7.41(s, 1H), 6.84 (t, J=54.1 Hz, 1H), 5.99 (d, J=7.2 Hz, 1H), 3.99 (s, 3H),1.63 (s, 3H).

Example 84 Preparation of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(1-cyanocyclopropane-1-carboxamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 328)

To a mixture of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (Intermediate 10) (0.049 mmol),1-cyanocyclopropanecarboxylic acid (0.058 mmol), and(1-Cyano-2-ethoxy-2-oxoethylidenaminooxy)dimethylamino-morpholino-carbeniumhexafluorophosphate (0.058 mmol) in dichloromethane (0.5 mL) was addedN,N-diisopropylethylamine (0.097 mmol). The reaction was stirred for 48hours, then concentrated and purified by reverse-phase HPLC to provide(R)-1-(2,5-difluoropyridin-3-yl)ethyl (4-(5-(1-cyanocyclopropane-1carboxamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 328) (MS (m/z) 470.0 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ9.22 (s, 1H), 8.96 (d, J=1.5 Hz, 1H), 8.11-7.67 (m, 2H), 5.95 (d, J=6.8Hz, 1H), 4.01 (s, 3H), 1.88-1.80 (m, 2H), 1.80-1.72 (m, 2H), 1.62 (s,3H).

Example 85 Preparation of Compounds 286-287 and 329-332

Compounds 286-287 and 329-332 were generally synthesized accordingScheme C. For example, (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-(1-cyanocyclopropane-1-carboxamido)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 329) was prepared as follows.

Preparation of (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-(1-cyanocyclopropane-1-carboxamido)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 329)

Step 1: (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-((tert-butoxycarbonyl)amino)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

To a mixture of4-(5-((tert-butoxycarbonyl)amino)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid (Intermediate 9) (0.62 mmol) in THF (5 mL) was added T3P (50% inDMF, 0.94 mmol), TMS-N3 (0.67 mmol) and triethylamine (1.2 mmol). Themixture was heated at 70° C. for 30 minutes.(R)-1-(2-chloro-5-fluoropyridin-3-yl)ethan-1-ol (0.94 mmol) was addedand the solution was heated at 70° C. for 90 minutes. The reaction wascooled to room temperature, concentrated and purified by silica gelchromatography to provide (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-((tert-butoxycarbonyl)amino)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate.(MS (m/z) 493.2 [M+H]⁺).

Step 2: (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-aminopyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Intermediate 11)

4 M HCl in 1,4-dioxane (20 mmol) was added to(R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-((tert-butoxycarbonyl)amino)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(0.49 mmol). The resulting suspension was stirred at RT for 18 hours.The reaction was concentrated to afford(R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-aminopyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate asthe hydrochoride salt (Intermediate 11). (MS (m/z) 393.1 [M+H]⁺).

Step 3: (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-(1-cyanocyclopropane-1-carboxamido)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

A vial was charged with (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-aminopyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (0.05 mmol) (Intermediate 11),1-cyanocyclopropane-1-carboxylic acid (0.06 mmol),N-ethyl-N′-(3-dimethylaminopropyl) carbodiimide hydrochloride (0.07mmol) and pyridine (2 mL). The reaction mixture was stirred at RT for 18hours, concentrated and purified by reverse phase HPLC to provide(R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-(1-cyanocyclopropane-1-carboxamido)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate.(MS (m/z) 486.2 [M+H]⁺). 1H NMR (400 MHz, DMSO-d6) δ 10.45 (s, 1H), 9.98(bs, 1H), 8.99 (s, 2H), 8.43 (bs, 1H), 7.94 (bs, 1H), 5.82 (bs, 1H),3.91 (s, 3H), 1.84-1.68 (m, 4H), 1.55 (bs, 3H).

Compounds 286-287 and 329-332 (Table 5) were similarly preparedaccording to Scheme C, Step 4 by reacting(R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-aminopyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (Intermediate 11) with the Reagent listed in Table 4 inplace of 1-cyanocyclopropane-1-carboxylic acid.

Compounds 286-287 were prepared using a mixture of(1S,2S)-1-cyano-2-(difluoromethyl)cyclopropane-1-carboxylic acid and(1R,2R)-1-cyano-2-(difluoromethyl)cyclopropane-1-carboxylic acid,followed by chiral SFC purification.

TABLE 5 Compounds prepared according to Scheme C. LCMS Compound No.Structure Reagent m/z 1H NMR Compound 286(R)-1-(2-chloro-5-fluoropyridin-3- yl)ethyl (4-(5-((1R,2R)-1-cyano-2-(difluoromethyl)cyclopropane-1- carboxamido)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

536.0 1H NMR (400 MHz, DMSO-d6) δ 10.67 (bs, 1H), 9.99 (bs, 1H), 8.98(s, 2H), 8.44 (bs, 1H), 7.94 (bs, 1H), 6.23 (ddd, J = 55.6, 54.3, 5.3Hz, 1H), 5.83 (bs, 1H), 3.91 (s, 3H), 2.82-2.58 (m, 1H), 2.20-2.11 (m,1H), 2.11-2.00 (m, 1H), 1.54 (bs, 3H). Compound 287(R)-1-(2-chloro-5-fluoropyridin-3- yl)ethyl (4-(5-((1S,2S)-1-cyano-2-(difluoromethyl)cyclopropane-1- carboxamido)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

536.0 1H NMR (400 MHz, DMSO-d6) δ 10.66 (s, 1H), 9.98 (bs, 1H), 8.99 (s,2H), 8.44 (s, 1H), 7.94 (bs, 1H), 6.23 (ddd, J = 55.6, 54.3, 5.3 Hz,1H), 5.83 (bs, 1H), 3.92 (s, 3H), 2.81-2.59 (m, 1H), 2.19-2.11 (m, 1H),2.11-2.02 (m, 1H), 1.54 (m, 3H). Compound 329(R)-1-(2-chloro-5-fluoropyridin-3- yl)ethyl(4-(5-(1-cyanocyclopropane-1- carboxamido)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

486.2 1H NMR (400 MHz, DMSO-d6) δ 10.45 (s, 1H), 9.98 (bs, 1H), 8.99 (s,2H), 8.43 (bs, 1H), 7.94 (bs, 1H), 5.82 (bs, 1H), 3.91 (s, 3H),1.84-1.68 (m, 4H), 1.55 (bs, 3H). Compound 330(R)-1-(2-chloro-5-fluoropyridin-3- yl)ethyl (4-(5-(3-fluorobicyclo[1.1.1]pentane-1- carboxamido)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

505.2 1H NMR (400 MHz, DMSO-d6) δ 10.18 (s, 1H), 9.91 (bs, 1H), 9.02 (s,2H), 8.43 (bs, 1H), 7.94 (bs, 1H), 5.82 (bs, 1H), 3.91 (s, 3H), 2.45 (d,J = 2.5 Hz, 6H), 1.54 (bs, 3H). Compound 331(R)-1-(2-chloro-5-fluoropyridin-3- yl)ethyl (1-methyl-4-(5-((1R,2R)-2-(trifluoromethyl)cyclopropane-1- carboxamido)pyrimidin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

529.0 1H NMR (400 MHz, DMSO-d6) δ 10.93 (s, 1H), 9.86 (bs, 1H), 8.97 (s,2H), 8.42 (bs, 1H), 7.93 (bs, 1H), 5.79 (bs, 1H), 3.91 (s, 3H),2.45-2.23 (m, 2H), 1.85-0.97 (m, 5H). Compound 332(R)-1-(2-chloro-5-fluoropyridin-3- yl)ethyl (1-methyl-4-(5-(6-(trifluoromethyl)nicotinamido)pyrimidin-2-yl)-1H-1,2,3-triazol-5-yl)carbamate

566.0 1H NMR (400 MHz, DMSO-d6) δ 11.05 (bs, 1H), 10.01 (bs, 1H), 9.31(d, J = 2.2 Hz, 1H), 9.16 (s, 2H), 8.63 (dd, J = 8.1, 2.2 Hz, 1H), 8.44(bs, 1H), 8.18 (d, J = 8.2 Hz, 1H), 7.94 (bs, 1H), 5.85 (d, J = 7.5 Hz,1H), 3.93 (s, 3H), 1.54 (bs, 3H).

Example 86 Preparation of (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-(3-fluorobicyclo[1.1.1]pentane-1-carboxamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 333)

Step 1: (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-((tert-butoxycarbonyl)amino)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

To a mixture of4-(5-((tert-butoxycarbonyl)amino)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid (0.62 mmol) in THF (5 mL) was added T3P (50% in DMF, 0.94 mmol),TMS-N3 (0.69 mmol) and triethylamine (1.2 mmol). The mixture was heatedat 70° C. for 30 minutes.(R)-1-(2-chloro-5-fluoropyridin-3-yl)ethan-1-ol (0.94 mmol) was addedand the solution was heated at 70° C. for 90 minutes. The reaction wascooled to RT, concentrated and purified by silica gel chromatography toprovide (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-((tert-butoxycarbonyl)amino)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate.(MS (m/z) 492.9. [M+H]⁺).

Step 2: (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-aminopyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

4 M HCl in 1,4-dioxane (14 mmol) was added to(R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-((tert-butoxycarbonyl)amino)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(0.34 mmol). The resulting suspension was stirred at RT for 18 hours.The reaction was concentrated to afford(R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-aminopyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate as thehydrochoride salt.

Step 3: (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-(3-fluorobicyclo[1.1.1]pentane-1-carboxamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

A vial was charged with (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-aminopyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (0.06 mmol), 3-fluorobicyclo[1.1.1]pentane-1-carboxylicacid (0.08 mmol), N-ethyl-N′-(3-dimethylaminopropyl) carbodiimidehydrochloride (0.12 mmol) and pyridine (2 mL). The reaction mixture wasstirred at RT for 18 hours, concentrated and purified by reverse phaseHPLC to provide (R)-1-(2-chloro-5-fluoropyridin-3-yl)ethyl(4-(5-(3-fluorobicyclo[1.1.1]pentane-1-carboxamido)pyrazin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate.(MS (m/z) 505.2 [M+H]⁺). 1H NMR (400 MHz, DMSO-d6) δ 10.92 (s, 1H),10.03 (bs, 1H), 9.20 (d, J=1.6 Hz, 1H), 8.92 (d, J=1.5 Hz, 1H), 8.43(bs, 1H), 7.94 (bs, 1H), 5.83 (bs, 1H), 3.92 (s, 3H), 2.47 (d, J=2.5 Hz,6H), 1.55 (bs, 3H).

Example 87 Preparation of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-((1r,3R)-3-cyano-3-methoxycyclobutane-1-carboxamido)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 334) and (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-((1s,3S)-3-cyano-3-methoxycyclobutane-1-carboxamido)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 335)

A mixture of the (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-aminopyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrochloride (0.048 mmol), 3-cyano-3-methoxycyclobutane-1-carboxylicacid (2eq), EDCI (2 eq) in pyridine (1 mL) was stirred 1 h at roomtemperature. After completion of the reaction, the residue was purifiedby prep-HPLC with Gilson prep HPLC (Gemini column, 30-95% CH₃CN in H₂Owith 0.1% TFA). Two peaks were isolated; the stereo structures arearbitrary assigned. Compound 334: (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-((1r,3R)-3-cyano-3-methoxycyclobutane-1-carboxamido)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate.(MS (m/z) 514.1 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ 9.06 (s, 2H),8.07 (m, 1H), 7.98-7.69 (m, 1H), 5.96 (m, 1H), 4.02 (s, 3H), 3.46 (s,2H) 2.99-2.79 (m, 2H), 2.76-2.48 (m, 2H), 1.63 (s, 3H). Compound 335:(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-((1s,3S)-3-cyano-3-methoxycyclobutane-1-carboxamido)pyrimidin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate.(MS (m/z) 514.1 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ 9.05 (s, 2H),8.05 (s, 1H), 7.97-7.75 (m, 1H), 5.96 (m, 1H), 4.01 (s, 3H), 3.55-3.49(m, 1H), 2.85 (m, 2H), 2.66 (m, 2H), 1.63 (s, 3H).

Example 88 Preparation of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(1-cyanocyclopropane-1-carboxamido)-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 336)

Step 1: Tert-butyl (6-bromo-5-fluoropyridin-3-yl)carbamate

To a solution of 6-bromo-5-fluoropyridin-3-amine (2.8 mmol) in THF (20mL) was added di-tert-butyl dicarbonate (5.7 mmol). The reaction washeated to 70° C. for 16 h concentrated and filtered through a plug ofsilica to provide the title compound which was used in the next stepwithout further purification.

Step 2:4-(5-((tert-butoxycarbonyl)amino)-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid

To a solution of 4-bromo-1-methyl-1H-1,2,3-triazole-5-carboxylic acid(1.3 mmol) in tetrahydrofuran (20 mL) at −70° C. was added a 1M solutionof lithium bis(trimethylsilyl)amide (1.5 mmol). After 15 minutes, a 2.5M solution of n-butyllithium (2.5 mmol) was added. After 1 hour, a 2 Msolution of zinc chloride (2.5 mmol) was added, and the reaction wasstirred at 15° C. for 30 minutes. At this point tert-butyl(6-bromo-5-fluoropyridin-3-yl)carbamate (1 mmol) and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (0.08 mmol)were added to the reaction and the reaction mixture was heated to 90° C.for 3 hours. After completion of the reaction, the reaction was cooledand diluted with 1M aqueous hydrogen chloride solution (20 mL). Thereaction mixture was extracted with ethyl acetate (30 mL×3). Thecombined organic layer was dried over sodium sulfate, concentrated,purified by column chromatography to provide4-(5-((tert-butoxycarbonyl)amino)-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid.

Step 3: tert-butyl(R)-(6-(5-(((1-(2,5-difluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)-5-fluoropyridin-3-yl)carbamate

4-(5-((tert-butoxycarbonyl)amino)-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazole-5-carboxylicacid (3.1 mmol), Azidotrimethylsilane (4.7 mmol), and T3P (50% in DMF)(4.7 mmol) was dissolved in THF (5 mL). Triethyl amine (9.4 mmol) wasadded dropwise at RT resulting in a clear solution after 5-30 minutes.((R)-1-(2,5-difluoropyridin-3-yl)ethan-1-ol (9.4 mmol) was added and thereaction was heated at 80° C. for 2 hours. Silica gel was then added andthe crude mixture was concentrated in vacuo and then purified by columnchromatography to afford tert-butyl(R)-(6-(5-(((1-(2,5-difluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)-5-fluoropyridin-3-yl)carbamate(0.6 mmol).

Step 4: (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-amino-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrogen chloride salt (Intermediate 12)

Tert-butyl(R)-(6-(5-(((1-(2,5-difluoropyridin-3-yl)ethoxy)carbonyl)amino)-1-methyl-1H-1,2,3-triazol-4-yl)-5-fluoropyridin-3-yl)carbamate(0.6 mmol) was suspended in 1.6 mL 4 M hydrochloric acid in dioxanes for1 hour. The mixture was then concentrated in vacuo to afford(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-amino-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrogen chloride salt (Intermediate 12) and was used without furtherpurification.

Step 5: (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(1-cyanocyclopropane-1-carboxamido)-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

To a mixture of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-amino-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatehydrogen chloride salt (0.07 mmol) in pyridine (1 mL) was added1-cyanocyclopropane-1-carboxylic acid (0.07 mmol) andN-ethyl-N′-(3-dimethylaminopropyl) carbodiimide hydrochloride (0.08mmol). The reaction mixture was left with magnetic stirring for 2 hoursat which point water (1 mL) was added the crude mixture was purified byHPLC to provide (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(1-cyanocyclopropane-1-carboxamido)-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate.(MS (m/z) 486.986 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ 8.78-8.52 (m,1H), 8.19-7.53 (m, 3H), 5.90 (d, J=6.8 Hz, 1H), 4.02 (s, 3H), 1.91-1.35(m, 7H).

Example 89 Preparation of ((R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(3-cyanobicyclo[1.1.1]pentane-1-carboxamido)-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 337)

(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(3-cyanobicyclo[1.1.1]pentane-1-carboxamido)-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

Prepared following Example 88 using3-cyanobicyclo[1.1.1]pentane-1-carboxylic acid (0.07 mmol) instead of1-cyanocyclopropane-1-carboxylic acid,(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(3-cyanobicyclo[1.1.1]pentane-1-carboxamido)-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatewas prepared. (MS (m/z) 513.010 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ8.61 (s, 1H), 8.25-7.51 (m, 3H), 5.89 (d, J=7.0 Hz, 1H), 4.01 (s, 3H),2.64 (s, 6H), 1.61 (s, 3H).

Example 90 Preparation of (R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(6-chloronicotinamido)-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate(Compound 338)

(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(6-chloronicotinamido)-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamate

Prepared following Example 88 using 6-chloronicotinic acid (0.07 mmol)instead of 1-cyanocyclopropane-1-carboxylic acid,(R)-1-(2,5-difluoropyridin-3-yl)ethyl(4-(5-(6-chloronicotinamido)-3-fluoropyridin-2-yl)-1-methyl-1H-1,2,3-triazol-5-yl)carbamatewas prepared. (MS (m/z) 532.975 [M+H]+). 1H NMR (400 MHz, Methanol-d4) δ8.98 (dd, J=2.5, 0.7 Hz, 1H), 8.73 (s, 1H), 8.38 (dd, J=8.4, 2.5 Hz,1H), 8.27 (dd, J=12.4, 2.1 Hz, 1H), 7.96 (d, J=78.6 Hz, 2H), 7.66 (dd,J=8.3, 0.8 Hz, 1H), 5.91 (d, J=6.8 Hz, 1H), 4.03 (s, 3H), 1.62 (s, 3H).

Example 91 Preparation ofrac-(1R,2R)-1-cyano-2-(difluoromethyl)cyclopropane-1-carboxylic acid

Step 1: (3,3-difluoroallyl)(phenyl)sulfane

NaH (153 mmol) was added to a 250 mL bottle under N₂. n-Hexane (50.0mL), was added and stirred at 25° C. for 5 minutes. n-hexane was removedby syringe. Dioxane (120 mL) was added to the reaction at 0° C. PhSH(118 mmol) was added to the mixture at 0° C., and stirred at 0° C. for0.5 hr. 3-bromo-3,3-difluoroprop-1-ene (177 mmol) was added to themixture at 0° C. The reaction as warmed to 25° C., and stirred at 25° C.for 1 hour. The reaction was quenched with sat. NH₄Cl (50.0 mL) at 0°C., and Extracted with ethyl acetate (100 mL*4). The organic phase waswashed with brine (100 mL), and dried over anhydrous Na₂SO₄. Thesolution was filtered and concentrated under vacuum. The residue waspurified by column chromatography to provide(3,3-difluoroallyl)(phenyl)sulfane.

Step 2: (E)-(3,3-difluoroprop-1-en-1-yl)(phenyl)sulfane

(3,3-difluoroallyl)(phenyl)sulfane (53.7 mmol) was dissolved in DMSO(20.0 mL) in a 100 mL bottle. t-BuOK (2.68 mmol) was added to themixture at 10° C. The mixture was warmed to 25° C., and stirred at 25°C. for 1 hr. The reaction was quenched with addition of H₂O (200 mL) at0-10° C. n-Hexane (100 mL) was added to the mixture, and the reactionwas extracted with n-hexane (200 mL*5). Wash the combined organic phasewith brine (100 mL), and dry over anhydrous Na₂SO₄. Filter andconcentrate under vacuum to obtain(E)-(3,3-difluoroprop-1-en-1-yl)(phenyl)sulfane.

Step 3: (E)-(3,3-difluoroprop-1-en-1-yl)diphenylsulfoniumtrifluoromethanesulfonate

Diphenyliodonium trifluoromethanesulfonate was added (48.8 mmol) to a250 mL bottle, and DCE (60.0 mL) was added.(E)-(3,3-difluoroprop-1-en-1-yl)(phenyl)sulfane (51.3 mmol) was added,followed by Cu powder (244 mmol) to the bottle at 10° C. The reactionwas stirred at 10-25° C. at 0.5 hr before immersing in a pre-heated oilbath (80° C.), and stirred for 2 hrs. The reaction was cooled to 20° C.and then filtered through a celite pad and washed with DCM (80 mL*4).The filtrate was concentrated and purified by column chromatography(SiO2, DCM/Acetone=100/1 to 20/1, Rf=0.50) to obtain(E)-(3,3-difluoroprop-1-en-1-yl)diphenylsulfoniumtrifluoromethanesulfonate.

Step 4: rac-2-ethoxyethyl(1R,2R)-1-cyano-2-(difluoromethyl)cyclopropane-1-carboxylate

2-Ethoxyethyl 2-cyanoacetate (63.6 mmol) in actone (100 mL) was added toa 250 mL bottle at 25° C. K₂CO₃ (191 mmol) was added followed by(E)-(3,3-difluoroprop-1-en-1-yl)diphenylsulfoniumtrifluoromethanesulfonate (70.0 mmol) to the bottle at 25° C. andstirred for 1 hour. The reaction was filtered through a celite pad andwashed with DCM (100 ml*3). Concentrated the organic phase under vacuum,and purified by HPLC (column: Phenomenex luna C18 (250*70 mm, 15 μm);mobile phase: [water (0.1% TFA)-ACN]; B %: 25ACN %-55ACN %, 25 min). Theproduct fraction was adjusted to pH=6-7 with sat. NaHCO₃. The fractionwas concentrate under reduced pressure to remove ACN, then extractedwith ethyl acetate (200 mL*3), and dried over anhydrous Na₂SO₄. Filteredand concentrated under vacuum to afford crude product, which was furtherPurified by prep HPLC (column: Welch Ultimate XB-CN 250*70*10 μm; mobilephase: [Hexane-EtOH (0.1% NH₃·H₂O)]; B %: 1%-40%,15 min) andconcentrated to obtain rac-2-ethoxyethyl(1R,2R)-1-cyano-2-(difluoromethyl)cyclopropane-1-carboxylate.

Step 5: rac-(1R,2R)-1-cyano-2-(difluoromethyl)cyclopropane-1-carboxylicacid

rac-2-ethoxyethyl(1R,2R)-1-cyano-2-(difluoromethyl)cyclopropane-1-carboxylate (34.3 mmol)was added to a 100 mL bottle and suspended in THF (70.0 mL). LiOH·H₂O (2M, 34.30 mL) was added to the mixture at 10° C., and stirred at 10-25°C. for 3 hours. The pH was adjusted to 2 with HCl (1N). The reaction wasextracted with ethyl acetate (50.0 mL*6), and washed with brine (50.0mL). The organics were dried over Na₂SO₄, filtered and concentratedunder vacuum. The product was triturated with DCM (20.0 mL) and theprecipitate was collected with by vacuum filtration to providerac-(1R,2R)-1-cyano-2-(difluoromethyl)cyclopropane-1-carboxylic acid.

Example 92 Preparation ofrac-(1S,2S)-1-cyano-2-fluorocyclopropane-1-carboxylic acid

Step 1: trimethyl((phenylthio)ethynyl)silane

Ethynyltrimethylsilane (1.43 mol) in THF (1000 mL), was added n-BuLi(2.5 M, 570 mL, 1.43 mol) dropwise at −78° C. The reaction was stirredat −78° C. for 30 mins and then a solution of 1,2-diphenyldisulfane(1.43 mol) in THF (400 mL) was added at −78° C. dropwise. After stirringfor 30 minutes at −78° C., the reaction was warmed up to 15° C. and stirfor 5 hours. The reaction was cooled to 0° C. and H₂O was added (500 mL)dropwise at 0° C. The reaction was extracted with EtOAc (500 mL*2), andthe aqueous layer is poured into NaClO. The combined organic layers werewashed with 0.1M NaOH (500 mL*3), H₂O (500 mL), dried over Na₂SO₄,filtered and concentrated in vacuo. The residue was used in the nextstep directly without purification to obtaintrimethyl((phenylthio)ethynyl)silane.

Step 2: ethynyl(phenyl)sulfane

Trimethyl((phenylthio)ethynyl)silane (1.28 mol) was added into MeOH(2000 mL). A mixture of K₂CO₃ (2.56 mol) in H₂O (600 mL) was addeddropwise at 15° C., and stirred for 16 hour. After concentration toremove MeOH, EtOAc (400 mL) and H₂O (200 mL) was added. Separated andthe aqueous layer extracted with EtOAc (200 mL*2). The combined organiclayers were dried over Na₂SO₄, filtered and concentrated in vacuo. Theresidue was purified by column chromatography to obtainethynyl(phenyl)sulfane.

Step 3: (1-fluorovinyl)(phenyl)sulfane

Ethynyl(phenyl)sulfane (1.16 mol), Pyr. (3.31 mol) was added into DCM(1000 mL). HF/Pyr. (4.62 mol) was added at 0° C., and then the reactionwas warmed to 15° C. and stirred for 10 mins. Sat. NaHCO₃ and NaHCO₃solid were added slowly to adjust pH=8. The organic layer was separated,washed with brine (1000 mL), dried over Na₂SO₄, filtered, andconcentrated in vacuo. The residue was purified by column chromatographyto obtain (1-fluorovinyl)(phenyl)sulfane.

Step 4: (1-fluorovinyl)diphenylsulfonium trifluoromethanesulfonate

(1-Fluorovinyl)(phenyl)sulfane (272 mmol) was suspended into DCE (400mL). Diphenyliodonium trifluoromethanesulfonate (258 mmol) and Cu (1.36mol) were added at 15° C. The reaction was heated to 100° C. and stirredfor 30 mins. The reaction was cooled to 15° C., filtered and the filtercake washed with DCM (100 mL). The filtrate was concentrated in vacuo,and the residue purified by column chromatography to obtain(1-fluorovinyl)diphenylsulfonium trifluoromethanesulfonate.

Step 5: rac-ethyl (1S,2S)-1-cyano-2-fluorocyclopropane-1-carboxylate

Ethyl 2-cyanoacetate (78.8 mmol) was added into MeCN (180 mL). DBU (94.6mmol) was added at 15° C. and stirred for 10 min followed by theaddition of (1-fluorovinyl)diphenylsulfonium trifluoromethanesulfonate(78.8 mmol) at 15° C. portion wise. After stirring at 15° C. for 30minutes the reaction was quenched with addition of sat. NH₄Cl (50 mL).The mixture was extracted with Ethyl Acetate (100 mL) two times and thecombined organic layers dried over Na₂SO₄, filtered and concentrated invacuo. The residue was purified by column chromatography to obtainrac-ethyl (1S,2S)-1-cyano-2-fluorocyclopropane-1-carboxylate.

Step 6: rac-(1S,2S)-1-cyano-2-fluorocyclopropane-1-carboxylic acid

rac-Ethyl (1S,2S)-1-cyano-2-fluorocyclopropane-1-carboxylate (14.0 mmol)was suspended into MeCN (11.0 mL) and H₂O (2.00 mL). Triazabicyclodecene(29.4 mmol) was added at 15° C. and stirred for 1 hr. The reaction wasextract with DCM (20 mL), and the aqueous layer was adjusted pH to 1-3by HCl (4M). The aqueous layer was extract with EtOAc (20 mL*3). Thecombined organic layers were dried over Na₂SO₄, filtered andconcentrated in vacuo. The residue was purified by column chromatographyto obtain rac-(1S,2S)-1-cyano-2-fluorocyclopropane-1-carboxylic acid.

Example 93 Calcium Assay

In vitro LPAR1 activity was measured in an intracellular calciummobilization assay.

CHO-K1 EDG2 cells (DiscoverX cat #93-0644C2) expressing human LPAR1(NM_001401.3) were seeded in a total volume of 25 μL of Dulbecco'sModification of Eagle's Medium (DMEM) with 10% Fetal Bovine Serum, 1×PenStrepGlutamine, 300 μg/ml Hygromycin, and 800 μg/ml G418 into384-well tissue culture plate (Grenier #781091) at 15,000 cells/well andincubated at 37° C. overnight. Prior to testing, 25 μL Calcium LoadingDye Component A (FLIPR Calcium 6 Assay Kit Molecular Device #R8190) and2.5 mM Probenecid (Invitrogen #P36400, prepared fresh) in Hank'sBalanced Salt Solution (Corning #21-023-CV), 20 mM HEPES (Corning#25-060-CI), 0.1% Bovine Serum Albumin (Sigma-Aldrich #A7906-500G) wasadd to the cells for 60 minutes at 37° C.

Agonist dose curves of LPA 18:2 (Avanti Polar Lipids cat #857138, 0.5 nMto 10 μM) were recorded to determine the LPA 18:2 EC₈₀ for subsequentantagonist assays. For agonist dose curves, cells were removed from theincubator 2 hours after dye loading and transferred to the FLIPR Tetrainstrument (Molecular Devices, San Jose, Calif.). Calcium mobilizationwas monitored for 5 min and 10 μL 6× LPA in HBSS/20 mM Hepes/0.1% bovineserum albumin (BSA) was added to the cells 5 seconds into the assay.

To determine the LPAR1 antagonist activity of test compounds, cells werepre-incubated with test compound at a dose range of 0.5 nM to 10 μM,followed by LPA at EC₈₀ concentration (100 nM). After dye loading, cellswere removed from the incubator and 0.3 μL of 200× antagonist was added.Cells were incubated for 60 minutes at 37° C. Antagonist activity wasmeasured on a FLIPR Tetra. Calcium mobilization was monitored for 3.5minutes and 10 μL 6× EC₈₀ LPA in HBSS, 20 mM HEPES, and 0.1% BSA wasadded to the cells 5 seconds into the assay. Signal amplitude (Maximumminus minimum) values were plotted against log₁₀ of antagonistconcentration using Dose Response Tool (Gilead Sciences Inc.) todetermine EC₅₀.

To assess the antagonistic potential of exemplified compounds EC₅₀values were determined for Compounds 1 to 338 in the LPAR1 calciummobilization assay. Results are shown in Table 6 (LPAR1 EC₅₀). Thecompound numbers correspond to the compound numbers in Examples 1 to 92.N/A=not available.

TABLE 6 LPAR1 Compound (EC₅₀; nM) Compound 1 6519.3 Compound 2 953.0Compound 3 10000 Compound 4 10000 Compound 5 1505.8 Compound 6 1859.6Compound 7 315.1 Compound 8 154.3 Compound 9 2696.7 Compound 10 1024.1Compound 11 731.2 Compound 12 540.8 Compound 13 148.1 Compound 14 1202.9Compound 15 452.1 Compound 16 2185.0 Compound 17 29.3 Compound 18 1129.3Compound 19 275.5 Compound 20 N/A Compound 21 39.6 Compound 22 43.4Compound 23 1105.0 Compound 24 N/A Compound 25 2268.3 Compound 26 587.4Compound 27 1277.1 Compound 28 29.1 Compound 29 261.4 Compound 30 516.2Compound 31 2334.4 Compound 32 798.9 Compound 33 1018.3 Compound 34428.9 Compound 35 103.1 Compound 36 112.4 Compound 37 54.6 Compound 3810000 Compound 39 50.8 Compound 40 75.2 Compound 41 38.1 Compound 42201.1 Compound 43 497.2 Compound 44 165.0 Compound 45 40.8 Compound 4629.7 Compound 47 19.1 Compound 48 22.8 Compound 49 353.2 Compound 501761.4 Compound 51 88.7 Compound 52 621.9 Compound 53 1456.0 Compound 547863.3 Compound 55 477.7 Compound 56 1135.1 Compound 57 339.2 Compound58 205.2 Compound 59 263.7 Compound 60 140.4 Compound 61 134.4 Compound62 109.8 Compound 63 120.4 Compound 64 76.4 Compound 65 81.9 Compound 6666.6 Compound 67 30.8 Compound 68 40.8 Compound 69 53.0 Compound 70 47.8Compound 71 89.7 Compound 72 17.0 Compound 73 17.3 Compound 74 1344.4Compound 75 23.4 Compound 76 274.7 Compound 77 25.5 Compound 78 83.6Compound 79 16.0 Compound 80 109.1 Compound 81 22.8 Compound 82 20.4Compound 83 343.7 Compound 84 14.5 Compound 85 11.2 Compound 86 16.6Compound 87 16.1 Compound 88 8.6 Compound 89 312.3 Compound 90 73.5Compound 91 187.0 Compound 92 601.4 Compound 93 133.0 Compound 94 4817.8Compound 95 308.6 Compound 96 2328.6 Compound 97 395.4 Compound 98 720.5Compound 99 53.9 Compound 100 90.8 Compound 101 1041.5 Compound 102 85.6Compound 103 16.6 Compound 104 559.9 Compound 105 1582.1 Compound 1061758.3 Compound 107 10000 Compound 108 419.6 Compound 109 1711.0Compound 110 68.2 Compound 111 190.9 Compound 112 1405.0 Compound 113775.1 Compound 114 504.4 Compound 115 654.2 Compound 116 322.5 Compound117 1143.9 Compound 118 1336.6 Compound 119 49.9 Compound 120 2466.1Compound 121 264.1 Compound 122 122.9 Compound 123 625.6 Compound 1243629.6 Compound 125 2711.3 Compound 126 1826.3 Compound 127 415.7Compound 128 309.4 Compound 129 492.5 Compound 130 271.3 Compound 131260.4 Compound 132 196.9 Compound 133 343.9 Compound 134 448.9 Compound135 725.7 Compound 136 602.5 Compound 137 1092.3 Compound 138 84.9Compound 139 123.2 Compound 140 349.3 Compound 141 459.3 Compound 142217.4 Compound 143 188.7 Compound 144 36.1 Compound 145 184.0 Compound146 271.0 Compound 147 33.9 Compound 148 30.4 Compound 149 328.7Compound 150 879.5 Compound 151 3151.9 Compound 152 3987.9 Compound 153932.6 Compound 154 667.8 Compound 155 748.4 Compound 156 50.7 Compound157 74.5 Compound 158 117.1 Compound 159 393.6 Compound 160 1454.9Compound 161 66.8 Compound 162 84.7 Compound 163 32.6 Compound 164 245.0Compound 165 487.1 Compound 166 238.5 Compound 167 99.4 Compound 16816.2 Compound 169 190.6 Compound 170 31.8 Compound 171 140.5 Compound172 236.1 Compound 173 181.0 Compound 174 106.6 Compound 175 35.4Compound 176 253.3 Compound 177 48.3 Compound 178 140.1 Compound 17946.5 Compound 180 122.7 Compound 181 428.4 Compound 182 2046.8 Compound183 1059.1 Compound 184 81.8 Compound 185 1704.2 Compound 186 100.5Compound 187 1236.1 Compound 188 451.9 Compound 189 989.3 Compound 190359.3 Compound 191 620.2 Compound 192 10000 Compound 193 287.1 Compound194 832.3 Compound 195 1538.5 Compound 196 1029.5 Compound 197 5.2Compound 198 613.1 Compound 199 65.7 Compound 200 94.0 Compound 201145.8 Compound 202 5.0 Compound 203 94.8 Compound 204 132.2 Compound 2058.3 Compound 206 71.8 Compound 207 41.2 Compound 208 21.1 Compound 20917.7 Compound 210 243.2 Compound 211 37.4 Compound 212 56.4 Compound 213175.3 Compound 214 356.8 Compound 215 1995.6 Compound 216 22.4 Compound217 58.1 Compound 218 24.0 Compound 219 37.7 Compound 220 157.5 Compound221 374.3 Compound 222 41.7 Compound 223 118.5 Compound 224 40.2Compound 225 16.3 Compound 226 183.8 Compound 227 205.5 Compound 228403.3 Compound 229 863.9 Compound 230 26.7 Compound 231 411.7 Compound232 1106.2 Compound 233 190.1 Compound 234 136.4 Compound 235 26.5Compound 236 1657.6 Compound 237 19.3 Compound 238 52.5 Compound 23962.3 Compound 240 N/A Compound 241 110.7 Compound 242 63.3 Compound 24371.9 Compound 244 130.8 Compound 245 11.7 Compound 246 103.4 Compound247 13.0 Compound 248 29.8 Compound 249 536.9 Compound 250 276.2Compound 251 38.5 Compound 252 73.5 Compound 253 550.7 Compound 254 18.1Compound 255 346.3 Compound 256 209.4 Compound 257 442.7 Compound 25819.3 Compound 259 101.0 Compound 260 160.7 Compound 261 11.9 Compound262 23.7 Compound 263 691.3 Compound 264 202.6 Compound 265 19.5Compound 266 748.6 Compound 267 588.2 Compound 268 7.3 Compound 269126.9 Compound 270 167.7 Compound 271 228.6 Compound 272 162.2 Compound273 248.2 Compound 274 403.2 Compound 275 241.0 Compound 276 139.9Compound 277 954.8 Compound 278 809.5 Compound 279 97.4 Compound 28098.7 Compound 281 86.6 Compound 282 1186.8 Compound 283 82.4 Compound284 907.9 Compound 285 71.8 Compound 286 104.3 Compound 287 1426.5Compound 288 33.5 Compound 289 21.5 Compound 290 10.9 Compound 291 157.2Compound 292 143.1 Compound 293 27.3 Compound 294 238.3 Compound 295391.0 Compound 296 46.9 Compound 297 354.1 Compound 298 1254.5 Compound299 4991.0 Compound 300 960.8 Compound 301 66.9 Compound 302 669.3Compound 303 565.4 Compound 304 46.4 Compound 305 1004.0 Compound 30699.7 Compound 307 N/A Compound 308 336.5 Compound 309 132.8 Compound 310453.9 Compound 311 1533.2 Compound 312 1528.3 Compound 313 51.8 Compound314 2.9 Compound 315 12.7 Compound 316 41.6 Compound 317 90.5 Compound318 9.5 Compound 319 1496.6 Compound 320 130.9 Compound 321 309.1Compound 322 169.5 Compound 323 177.5 Compound 324 53.7 Compound 325185.1 Compound 326 304.9 Compound 327 255.2 Compound 328 1132.7 Compound329 749.2 Compound 330 599.6 Compound 331 22.8 Compound 332 354.1Compound 333 219.3 Compound 334 3418.0 Compound 335 778.4 Compound 336257.5 Compound 337 163.2 Compound 338 132.0

Unless otherwise defined, all technical and scientific terms used hereinhave the same meaning as commonly understood by one of ordinary skill inthe art to which this disclosure belongs.

Thus, it should be understood that although the present disclosure hasbeen specifically disclosed by preferred embodiments and optionalfeatures, modification, improvement and variation of the disclosuresembodied therein herein disclosed may be resorted to by those skilled inthe art, and that such modifications, improvements and variations areconsidered to be within the scope of this disclosure. The materials,methods, and examples provided here are representative of preferredembodiments, are exemplary, and are not intended as limitations on thescope of the disclosure.

The disclosure has been described broadly and generically herein. Eachof the narrower species and subgeneric groupings falling within thegeneric disclosure also form part of the disclosure. This includes thegeneric description of the disclosure with a proviso or negativelimitation removing any subject matter from the genus, regardless ofwhether or not the excised material is specifically recited herein.

In addition, where features or aspects of the disclosure are describedin terms of Markush groups, those skilled in the art will recognize thatthe disclosure is also thereby described in terms of any individualmember or subgroup of members of the Markush group.

It is to be understood that while the disclosure has been described inconjunction with the above embodiments, that the foregoing descriptionand examples are intended to illustrate and not limit the scope of thedisclosure. Other aspects, advantages and modifications within the scopeof the disclosure will be apparent to those skilled in the art to whichthe disclosure pertains.

1.-179. (canceled)
 180. A compound that is of the formula:

or a pharmaceutically acceptable salt thereof.
 181. A compound of theformula:

or a pharmaceutically acceptable salt thereof.
 182. A compound of theformula:

or a pharmaceutically acceptable salt thereof.
 183. A compound of theformula:

or a pharmaceutically acceptable salt thereof.
 184. A compound of theformula:

or a pharmaceutically acceptable salt thereof.